Reemerging Nutritional Rickets: A Historical Perspective | Geriatrics | JAMA Pediatrics | JAMA Network
[Skip to Navigation]
Sign In
April 2005

Reemerging Nutritional Rickets: A Historical Perspective

Author Affiliations

Author Affiliations: Department of Pediatrics, University of Pittsburgh School of Medicine and Children’s Hospital of Pittsburgh (Dr Rajakumar), and Center for Minority Health, University of Pittsburgh, Graduate School of Public Health (Dr Thomas), Pittsburgh, Pa.

Arch Pediatr Adolesc Med. 2005;159(4):335-341. doi:10.1001/archpedi.159.4.335

Recent case reports highlight the resurgence of rickets in certain groups of breastfed infants. Infants residing in the North, irrespective of skin color, and dark-skinned African American infants residing anywhere in the United States are most vulnerable to nutritional rickets if they are exclusively breastfed past age 6 months without vitamin D supplementation. At the turn of the 20th century, rickets was nearly universal among African American infants living in the North. The discovery of vitamin D, the initiation of public health campaigns to fortify infant foods with vitamin D, and the supplementation of vitamin D to breastfed infants were responsible for overcoming the rickets scourge. We review a classic nutritional study by Alfred F. Hess, one of the greatest clinical nutritional researchers of the early 20th century, in the context of the resurgence of rickets, especially among dark-skinned infants. The Columbus Hill district, a black community of New York, NY, served as the setting for the study. Sixty-five infants (aged 1-17 months) entered a 6-month open-label trial of daily cod liver oil therapy. Participants were assessed for signs of rickets at recruitment and at 2, 4, and 6 months. Cod liver oil prevented the development of rickets in 34 (92%) of 37 infants treated for 6 months and in 7 (58%) of 12 treated for 4 months. Of the 16 infants who did not take the prescribed treatment, rickets progressed unremittingly in 15. Hess translated his success into a public health campaign leading to the development of the first rickets clinic in 1917. This was the first step in the conquest of the rickets epidemic of the early 20th century.

Nutritional rickets, an apparently vanquished disease in the United States, is back in the limelight and has resurfaced as a public health issue. In 2003, in response to the problem of reemerging rickets, the American Academy of Pediatrics revised its policy on vitamin D supplementation to infants and children.1 Several recently reported case series2-5 have highlighted the vulnerability of the breastfed African American infant to the development of nutritional rickets. The common theme among the recently reported cases of nutritional rickets in North America and the United Kingdom is that most affected infants are dark skinned (African American, Afro-Caribbean, or Asian descent)2-6 or residents of northern latitudes who had been exclusively breastfed beyond 6 months of age without vitamin D supplementation.7,8 Several of the reports were from North Carolina and Georgia, relatively sunny southern states considered to be at low risk for seasonal hypovitaminosis D.2-4 In the context of the reemergence of nutritional rickets, we review a classic nutritional study by Alfred Hess that explores the prophylactic role of cod liver oil in the eradication of nutritional rickets in African American infants.

Vitamin d photosynthesis and the history of rickets

The propensity for dark-skinned breastfed infants to develop rickets stems from the fact that people mostly meet their vitamin D needs from exposure to sunlight and that breast milk per se is a poor source of vitamin D.1,9,10 Vitamin D, the sunshine vitamin, is a hormone.11,12 On exposure to UV-B rays (290-315 nm), 7-dehydrocholesterol, the vitamin D precursor in the skin, gets photolyzed to previtamin D3. Previtamin D3 is thermally isomerized to vitamin D3 (cholecalciferol).9,12 Vitamin D3 undergoes further hydroxylation in the liver and kidney to become the active form of vitamin D (1,25-dihydroxyvitamin D or calcitriol).9,12 Endogenous vitamin D production in the skin is affected by the geographic latitude of residence, the degree of skin pigmentation, the season of the year, clothing, atmospheric pollution, and the application of sunscreen.9,11,12

Of the several determinants of endogenous vitamin D production, geographic latitude of residence and skin pigmentation are the dominant factors. Residents of higher latitudes are vulnerable to seasonal hypovitaminosis D during the winter months owing to inadequate sunlight exposure.12-15 In northern latitudes, the zenith angle of the sun is increased during winter, and the consequent oblique trajectory through the ozone stratosphere results in fewer UV-B rays reaching the earth’s surface. Webb et al15 showed that the winter sun is ineffective at producing cutaneous vitamin D between November and February in Boston, Mass (42° N), and between October and March in Edmonton, Alberta (52° N). The basis for the role of skin pigmentation in endogenous vitamin D production stems from the function of melanin. Epidermal melanin content determines the variation in skin color of various race groups. The highest concentration of 7-dehydrocholesterol, the vitamin D precursor, is in the deeper layers of the epidermis (stratum spinosum and stratum basale).16 Melanin competes with 7-dehydrocholesterol for the UV-B photons and preferentially absorbs the necessary UV-B rays needed for vitamin D synthesis.17 Hence, individuals with darkly pigmented skin who reside in the North are most vulnerable to seasonal vitamin D deficiency during winter.18

At the turn of the 20th century, rickets was rampant among infants residing in the northern industrialized cities in the United States. The exact cause of rickets was debated. Faulty diet, faulty environment (poor hygiene and lack of fresh air and sunshine), and lack of exercise were all implicated in the cause of rickets.19 Scientific progress to solve the rickets malady was at its peak during the early part of the 20th century. Mellanby,20 McCollum et al,21 and Shipley et al22 induced rickets in animal models and demonstrated the curative property of cod liver oil in healing the induced experimental rickets. In 1922, McCollum et al23 showed that heated cod liver oil loses its antixerophthalmic property but not its antirachitic function, and they named the antirachitic factor vitamin D because it was the fourth vitamin to be described. In 1919, just as dietary vitamin D was being discovered, Kurt Huldschinsky cured rickets in infants by exposing them to a mercury vapor lamp.24,25 Soon afterward, clinical experiments confirmed the curative and preventive properties of cod liver oil in the management of rickets.26 In 1924, Hess and Harry Steenbock independently discovered that UV irradiation of various foods, such as milk, oils, and cereals, could render them with antirachitic properties by the activation of ergosterol.27 Irradiated ergosterol soon became readily available as a potent vitamin D source for food fortification and the treatment of rickets.28 The public health initiative of the fortification of cow’s milk–based infant formulas with vitamin D and vitamin D supplementation of breastfed infants became common practice by the 1930s, resulting in the near disappearance of rickets in the United States by the 1960s.28-30

Role of breastfeeding and sunlight

The reemergence of rickets has coincided with the resurgence of breastfeeding.28,29,31 The promotion of breastfeeding without emphasizing the need for vitamin D supplementation for the prevention of rickets has led to the resurgence of this nutritional disorder in a vulnerable pouplation.28 Most recently reported cases of rickets occurred in breastfed African American infants.2-5

Despite the increased prevalence of nutritional rickets among African American infants, rickets is a color-blind disease.2-5 Breast milk is a poor source of vitamin D.9 In the phase of no vitamin D supplementation, all breastfed infants are vulnerable to the development of rickets if they cannot photosynthesize their required levels of vitamin D. The public health message that infants younger than 6 months not be exposed to any direct sunlight to reduce their eventual risk of skin cancer, and the use of sunscreens and protective clothing among older infants to avoid exposure to direct sunlight, are also relevant factors in the resurgence of rickets.1 The risk of developing rickets is much greater among dark-skinned infants because they require a 6-fold greater exposure to sunlight to elevate their vitamin D levels to the same degree as seen in white infants.32 Cultural practices that limit exposure to sunlight also exacerbate the vulnerability to vitamin D deficiency.

In this context, we review a seminal study from 1917 by Hess and Unger33 entitled “Prophylactic Therapy for Rickets in a Negro Community.” This study explored the issue of the eradication of rickets in African American infants by the prophylactic administration of cod liver oil.


Nearly 85 years ago, Alfred F. Hess (Figure 1), in collaboration with Lester Unger, pioneered a community-based clinical study to evaluate the effectiveness of cod liver oil as a remedy in the preventive treatment of rickets.33 Until then, cod liver oil had been used only as a therapeutic agent in individual cases of infantile rickets. Having been aware that the rickets burden was highest among black infants, Hess and Unger chose the Columbus Hill district, a black community of New York, NY, to conduct their research. At the time of this study, rickets was pervasive among black infants. Hess and Unger observed: “It may be safely stated that 90% of colored babies have rickets, and that even a majority of those that breastfed show signs of this disorder.”33(p487)

Figure 1. 
Alfred F. Hess (1875-1933). Courtesy of the National Library of Medicine, Bethesda, Md.

Alfred F. Hess (1875-1933). Courtesy of the National Library of Medicine, Bethesda, Md.

The Henry Street Settlement (Figure 2) and the National League for the Study of the Urban Conditions of the Negro identified the Columbus Hill district as a needy neighborhood in terms of health disparities and economic woes.33,34 Hess and Unger summarized their plight as follows: “People pay high rents, earn low wages, and unfortunately have had but meager educational opportunities.”33(p487) The infant mortality statistics reflect the extent of the health burden faced by the residents of Columbus Hill. In 1915, when the infant mortality rate was 96 per 1000 in the white population and 202 per 1000 in the Negro infants of New York City, the Columbus Hill district’s infant mortality rate was 314 per 1000. Most infant deaths were due to respiratory illnesses such as pulmonary tuberculosis, whooping cough, and pneumonia, and rickets predisposed an infant to increased morbidity from such respiratory illnesses. Therefore, Hess and Unger proposed that the reduction of rickets could indirectly reduce the high infant mortality rate among Negro infants.

Figure 2. 
An early photograph of Henry Street Settlement. Courtesy of Henry Street Settlement, New York, NY.

An early photograph of Henry Street Settlement. Courtesy of Henry Street Settlement, New York, NY.


Sixty-five infants, 1 to 17 months of age, were studied for a 6-month period between December 1916 and June 1917. A visiting nurse familiar with the community helped the researchers access recruited patients in their homes throughout the study (Figure 3). Most of the enrolled infants had siblings with rickets at the time of recruitment. Patients were clinically assessed for rickets at the beginning of the study based on the presence or absence of craniotabes, rickety rosary, and epiphyseal widening, and the signs of rickets were divided into 4 grades of intensity (+ to ++++). Enrolled patients began daily therapy with cod liver oil for 6 months. Infants younger than 6 months were prescribed teaspoon (2.5 mL) of cod liver oil 3 times a day, and older infants were asked to take twice as much. Although cod liver oil was initially delivered to the homes of the infants, prescription refills were provided at a neighborhood settlement house each morning and 1 evening of the week. At recruitment, the mode of infant feeding (breastfeeding vs artificial feeding) and the dietary intake of the mothers were reviewed. Data regarding the time the family has spent in the North and the family’s socioeconomic strata were collected. The investigators evaluated the clinical status of rickets among the enrolled patients at 2, 4, and 6 months. The visiting nurse and the researchers frequently visited the families to monitor the health of the enrolled infants and assure themselves of the compliance with the prescribed treatment.

Figure 3. 
An African American visiting nurse holding an African American infant. Photograph from the Visiting Nurse Service Report for 1923, administered by the Henry Street Settlement. Courtesy of Henry Street Settlement Archives, University of Minnesota Libraries, Minneapolis.

An African American visiting nurse holding an African American infant. Photograph from the Visiting Nurse Service Report for 1923, administered by the Henry Street Settlement. Courtesy of Henry Street Settlement Archives, University of Minnesota Libraries, Minneapolis.


At the end of 6 months, the eligible patients were categorized into 3 treatment groups and 1 control group. The group categorization was based on the average cumulative amount of cod liver oil ingested by each infant in the group and the duration of therapy. Treatment group1 (n = 32) was compliant for 6 months, and each infant had an average cumulative total of 54 oz (1620 mL) of cod liver oil. Although treatment group 2 (n = 5) was also compliant for 6 months, the average cumulative intake of cod liver oil per infant was lower (23 oz [690 mL]). Infants belonging to treatment group 3 (n = 12) were compliant for only 4 months, and the average cumulative intake of cod liver per infant was 21 oz (630 mL). The control group comprised the 16 noncompliant infants who took no cod liver oil at all.

Prophylactic cod liver oil therapy successfully prevented the onset of rickets or resolved the signs of established rickets in 92% of infants treated for 6 months and in 58% of infants treated for 4 months (Table 1). Of the 16 untreated infants in the control group, 15 (94%) had progressive unremitting rickets at the end of 6 months (Table 1). This clear demarcation between the treatment and control groups, despite no alteration in the basal diets or mode of life or the provision of any other treatment besides cod liver oil, establishes the value of cod liver oil as an effective prophylactic agent against the development of rickets.

Table 1. 
Comparative Incidence of Rickets Among Infants Receiving and Not Receiving the Prophylactic Therapy*
Comparative Incidence of Rickets Among Infants Receiving and Not Receiving the Prophylactic Therapy*

Investigators depended on clinical examination alone to establish the diagnosis of rickets, assess its severity, and monitor its progress during the study. Neither radiographic nor biochemical monitoring of patients was common practice in the diagnostic evaluation of rickets in 1915. At the beginning of the study, the presence or absence of rickets was established, and the infants were reassessed at 2, 4, and 6 months for the progression, resolution, or development of rickets. Clinical rickets was evident in 59 (91%) of the 65 patients at study entry, and most of them were breastfed (48 of 65; 74%).

Hess and Unger observed: “Cod liver oil proved to be a more potent factor than breastfeeding in warding off rickets, and that almost all the colored babies developed rickets even though they were nursed”33(p489) (Table 2). In the control group, the group that received no cod liver oil, rickets progressed in 15 of the 16 infants, and neither breastfeeding nor artificial feeding afforded any protection against rickets.

Table 2. 
Relationships Among Mode of Feeding, Rickets Status, and Prophylactic Cod Liver Oil Therapy*
Relationships Among Mode of Feeding, Rickets Status, and Prophylactic Cod Liver Oil Therapy*


Hess and Unger concluded that cod liver oil was efficacious in protecting the Negro infant against the development of rickets. Although larger doses of cod liver oil offered more protection (54 vs 23 oz [1620 vs 690 mL]), Hess and Unger stated that it is the regularity and duration of administration (6 vs 4 months) that confers the protection against rickets. Infants who were not given prophylactic therapy invariably had progressive unremitting rickets.

Hess and Unger33 were aware of the seasonal vulnerability for the occurrence of rickets and chose the “colder season” for conducting their study. Acknowledging the seasonal limitation of their study and their previous experience with rickets, Hess and Unger stated that cod liver oil prophylactic treatment should be considered only during the colder season. Hess and Unger realized that many Negro infants residing in New York were afflicted with rickets and that neither breastfeeding nor artificial feeding offered any protection against the development of rickets. In an attempt to explain this racial predilection, they explored the role of maternal diet, culinary practices, and the immigration history of the residents of Columbus Hill.33,34

The Columbus Hill district was in Manhattan, on west 30th Street and the area around 7th Avenue, and had previously been called San Juan Hill.35,36 Most residents of Columbus Hill were migrants from the West Indies, and only a few of them were from the South. In their native West Indies, there was plenty of sunshine and an abundance of fresh vegetables and fruits.34 In contrast, New York City offered a distinct change in climate and diet. The Columbus Hill resident’s diet lacked fresh fruits, vegetables, and milk and offered plenty of meat.34 Rickets was rare among infants residing in the tropics. Hess and Unger34 confirmed directly from several physicians practicing in the West Indies and other parts of the tropics that rickets was rare among the native infants. They ventured to speculate that the contrast in the northern Negro’s mode of life, the change in the climate, and the marked difference in the food could all play a part in their excessive susceptibility to rickets.33

In this seminal study, Hess and Unger33 also demonstrate the successful essentials of recruitment of minorities in research participation and the establishment of effective public health initiatives in overcoming the rickets burden. The National League for the Study of the Urban Conditions of the Negro and the Henry Street Settlement had surveyed the Columbus Hill community to ascertain the socioeconomic conditions responsible for its high infant mortality rate. Lincoln House, a branch of Henry Street Settlement in the Columbus Hill neighborhood, had a reputation for social reform.36,37 Partnering with those organizations was essential for the building of trust between the community and the researchers, which enabled the researchers to gain access to the homes of the participants. The fact that the study nurse had worked in the district for several years previously was also a factor in helping build the trust between the participants and researchers and in gaining access to the homes of the participants.33 Conducting the study in an economically and medically vulnerable community where rickets was highly prevalent was essential for judging the impact of the intervention. The Syphilis Study at Tuskegee (1932-1972) used similar methods to build community trust, namely, hiring a black nurse (Eunice Rivers) to maintain cohesion and continuity for the project.38 Although it is desirable to build trust when working with vulnerable populations, we must be mindful of the potential for unintended consequences in the name of doing good.39

During the study, the dispensing station for cod liver oil evolved into a community-based rickets clinic. As the research progressed, community awareness of rickets increased, and Columbus Hill district mothers began to seek consultation for diagnosis and treatment of rickets at that clinic. Hess and Unger33 proposed setting up such “rickets clinics” in the Negro and Italian districts of large cities because rickets was equally prevalent among Italian infants. The proposed creation of the rickets clinic was modeled after the existing specialized clinics for treatment of malaria or tuberculosis, addressing the particular needs of the neighborhood.33 They suggested that existing milk or baby welfare stations would be suitable sites for the establishment of rickets clinics. As a direct result of the study by Hess and Unger,33 Commissioner Emerson of the Department of Health agreed to establish a rickets clinic during the fall of 1917 at the Columbus Hill district’s baby welfare station and to dispense cod liver oil at cost. As envisioned by Hess, the Department of Health, in collaboration with the Association for Improving the Condition of the Poor, established a rickets clinic during the fall of 1917.40 By 1921, the success of the Columbus Hill experiment was adapted by the Mulberry Health Center, located in an Italian neighborhood, and infants younger than 1 year were actively screened and treated for rickets.41 The Columbus Hill clinic emphasized maternal and child care throughout the early years and was accessed by 90% of the community by 1925.41

In this article, we celebrate Hess’s contribution as a clinical researcher and his ability to translate clinical research into public health and preventive medicine. Hess was a leading clinical researcher of the early 20th century. His pioneering work pertains to nutritional sciences. He demonstrated that oxidation of foods results in the loss of vitamin C.42 At the Hebrew Infant Asylum, Hess observed several cases of scurvy among infants fed pasteurized milk when orange juice had been excluded from their diets.43,44 He showed that the feeding of orange juice, raw milk, or potatoes could cure the scurvy.44 Hess recommended supplementation of fresh fruit or vegetable juices to infants fed heated milks to prevent scurvy.44 This led to the eradication of scurvy in the United States.

The contribution of Hess to the field of vitamin D nutrition is seminal. Besides successfully demonstrating the efficacy of cod liver oil as a prophylactic agent in the prevention of rickets, Hess also showed that infantile rickets could be cured by exposure to sunlight alone while the affected infant’s diet remained unchanged.33,42,45 Hess established the chemical basis for heliotherapy by demonstrating that the clinical cure of rickets by sunlight was associated with an increase in serum phosphate level, as noted with cod liver oil therapy.46 Hess’s greatest discovery came in 1924, when he showed that UV irradiation could render antirachitic function to certain foods.27,42 Windaus identified the antirachitic substance in irradiated foods as ergosterol in 1927, and the following year he was awarded the Nobel Prize for this discovery.42 Windaus acknowledged the influence of Hess’s work on his discovery in his acceptance speech.42

By the time Hess died in 1933, he had published 227 medical manuscripts and classic monographs on scurvy and rickets. At the time of his death, Hess was a foremost investigator among pediatricians in the United States.42 An eminent contemporary pediatrician described Hess as an “out post in the advance of scientific medicine.”42 In memory of Hess, Abraham Flexner states that “Hess put forth a whole series of publications of the greatest worth and value. Some of these have been outmoded by time; science has passed beyond them and their importance at the time of their appearance is no longer apparent. Others have great importance today.”42(pxxvii) Hess’s contribution to child health will always be revered; however, his ability to translate clinical knowledge into successful public health initiatives in the eradication of rickets is what we would like to reflect. We believe that reviewing this classic study by Hess at a time when rickets is reemerging as a disease to contend with among breastfed African American infants will inspire us to find ways to combat this problem.

Correspondence: Kumaravel Rajakumar, MD, Department of Pediatrics, Children’s Hospital of Pittsburgh, 3705 Fifth Ave, Pittsburgh, PA 15213-2583 (

Back to top
Article Information

Accepted for Publication: November 17, 2004.

Additional Information: Throughout the article, the terms Negro, black, colored, and African American are used interchangeably to reflect the nomenclature during the times in which these terms were used.

Acknowledgment: We thank Henry Street Settlement, New York, for providing the photographic material from their archives; Sari Weintraub of Henry Street Settlement and David Klassen, archivist and interim curator,Social Welfare History Archives, University of Minnesota Libraries, for their help with our research of the Henry Street Settlement’s archival material; Jeffrey Brosco of the Department of Pediatrics at the University of Miami School of Medicine, Miami, Fla, for suggestions and comments to help improve this manuscript; and an anonymous reviewer from the Archives of Pediatrics & Adolescent Medicine.

American Academy of Pediatrics, Prevention of rickets and vitamin D deficiency: new guidelines for vitamin D intake.  Pediatrics 2003;111908- 910PubMedGoogle ScholarCrossref
 Severe malnutrition among young children—Georgia, January 1997-June 1999.  MMWR Morb Mortal Wkly Rep 2001;50224- 227Google Scholar
Tomashek  KMNesby  SScanlon  KS  et al.  Nutritional rickets in Georgia.  Pediatrics 2001;107e45Google ScholarCrossref
Kreiter  SRSchwartz  RPKirkman  HN  JrCharlton  PACalikoglu  ASDavenport  ML Nutritional rickets in African-American breast-fed infants.  J Pediatr 2000;137153- 157PubMedGoogle ScholarCrossref
Biser-Rohrbaugh  AHadley-Miller  N Vitamin D deficiency in breast-fed toddlers.  J Pediatr Orthop 2001;21508- 511PubMedGoogle Scholar
Ladhani  SSrinivasan  LBuchanan  CAllgrove  J Presentation of vitamin D deficiency.  Arch Dis Child 2004;89781- 784PubMedGoogle ScholarCrossref
Eugster  EASane  KSBrown  DM Minnesota rickets: need for policy changes to support vitamin D supplementation.  Minn Med 1996;7929- 32PubMedGoogle Scholar
Binet  AKooh  SW Persistence of vitamin D deficiency rickets in Toronto in the 1990s.  Can J Public Health 1996;87227- 230PubMedGoogle Scholar
Institute of Medicine, Dietary Reference Intakes for Calcium, Phosphorus, Magnesium, Vitamin D, and Fluoride.  Washington, DC National Academy Press1997;251- 287
Committee on Nutrition; American Academy of Pediatrics, Vitamins: vitamin D Kleinman  REed. Pediatric Nutrition Handbook 4th ed. Elk Grove Village, Ill American Academy of Pediatrics1998;275- 277Google Scholar
Holick  MF Vitamin D: the underappreciated D-lightful hormone that is important for skeletal and cellular health.  Curr Opin Endocrinol Diabetes 2002;987- 98Google ScholarCrossref
Holick  MF McCollum Award Lecture, 1994: vitamin D: new horizons for the 21st century.  Am J Clin Nutr 1994;60619- 630PubMedGoogle Scholar
Stamp  TCRound  JM Seasonal changes in human plasma levels of 25-hydroxyvitamin D.  Nature 1974;247563- 565PubMedGoogle ScholarCrossref
McLaughlin  MRaggatt  PRFairney  ABrown  DJLester  EWills  MR Seasonal variations in serum 25-hydroxycholecalciferol in healthy people.  Lancet 1974;1536- 538Google ScholarCrossref
Webb  ARKline  LHolick  MF Influence of season and latitude on the cutaneous synthesis of vitamin D3: exposure to winter sunlight in Boston and Edmonton will not promote vitamin D3 synthesis in human skin.  J Clin Endocrinol Metab 1988;67373- 378Google ScholarCrossref
Holick  MFMacLaughlin  JAClark  MB  et al.  Photosynthesis of previtamin D3 in human skin and the physiologic consequences.  Science 1980;210203- 205PubMedGoogle ScholarCrossref
Norman  AW Sunlight, season, skin pigmentation, vitamin D, and 25-hydroxy vitamin D: integral component of vitamin D endocrine system.  Am J Clin Nutr 1998;671108- 1110PubMedGoogle Scholar
Harris  SSDawson-Hughes  B Seasonal changes in plasma 25-hydroxyvitamin D concentrations in young American black and white women.  Am J Clin Nutr 1998;671232- 1236PubMedGoogle Scholar
Rajakumar  K Vitamin D, Cod-liver oil, sunlight, and rickets: a historical perspective.  Pediatrics 2003;112e132- e135Google ScholarCrossref
Mellanby  E An experimental investigation on rickets.  Lancet 1919;1407- 412Google Scholar
McCollum  EVSimmonds  NParsons  HTShipley  PGPark  EA Studies on experimental rickets, I: the production of rachitis and similar diseases in the rat by deficient diets.  J Biol Chem 1921;45333- 342Google Scholar
Shipley  PGPark  EAMcCollum  EVSimmonds  NParsons  HT Studies on experimental rickets, II: the effect of cod liver oil administered to rats with experimental rickets.  J Biol Chem 1921;45343- 348Google Scholar
McCollum  EVSimmonds  NBecker  JEShipley  PG Studies on experimental rickets, XXI: an experimental demonstration of the existence of a vitamin which promotes calcium deposition.  J Biol Chem 1922;53293- 312Google Scholar
McCollum  EV A History of Nutrition.  Cambridge, Mass Riverside Press1957;
Chick  H The discovery of vitamins.  Prog Food Nutr Sci 1975;11- 20PubMedGoogle Scholar
Chick  DH Study of rickets in Vienna 1919-1922.  Med Hist 1976;2041- 51PubMedGoogle ScholarCrossref
Hess  AFLewis  JMRivkin  H Clinical experience with irradiated ergosterol.  JAMA 1928;91783Reprinted inHess  AF Collected Writings 2 Springfield, Ill Charles C Thomas1936;337- 349Google ScholarCrossref
Welch  TRBergstrom  WHTsang  RC Vitamin D–deficient rickets: the reemergence of the once conquered disease.  J Pediatr 2000;137143- 145PubMedGoogle ScholarCrossref
Chesney  RW Rickets: the third wave.  Clin Pediatr (Phila) 2002;41137- 139Google ScholarCrossref
Harrison  HE A tribute to the first lady of public health (Martha M. Eliot) V: The disappearance of rickets.  Am J Public Health Nations Health 1966;56734- 737PubMedGoogle ScholarCrossref
Ryan  AS The resurgence of breast-feeding in the United States.  Pediatrics 1997;99e12Google ScholarCrossref
Clemens  TLHenderson  SLAdams  JS  et al.  Increased skin pigment reduces the capacity of skin to synthesise vitamin D3 Lancet 1982;174- 76PubMedGoogle ScholarCrossref
Hess  AFUnger  LJ Prophylactic therapy for rickets in a Negro community.  JAMA 1917;691583Reprinted in:Hess  AF Collected Writings 1 Springfield, Ill Charles C Thomas1936;487- 494Google ScholarCrossref
Hess  AFUnger  LJ The diet of the Negro mother in New York City.  JAMA 1918;70- 900Reprinted in:Hess  AF Collected Writings 1 Springfield, Ill Charles C Thomas1936;500- 509Google Scholar
 Gotham comes of age: New York through the lens of the Byron Company, 1892-1942. Available at: March 26, 2004
Founding of Lincoln House, In: Year Book of the Henry Street Settlement and Its Branches, 1921: Lincoln House.  New York, NY Henry Street Settlement1921;58- 63
Lasch-Quinn  E The mainstream settlement movement and blacks.  Black Neighbors: Race and the Limits of Reform in the American Settlement House Movement, 1890-1945 Chapel Hill University of North Carolina Press1993;29- 46Google Scholar
Jones  J Bad Blood: The Tuskegee Syphilis Experiment.  New York Free Press1993;
Thomas  SQuinn  S The Tuskegee Syphilis Study 1932-1972: implications for HIV education and AIDS reduction programs in the black community.  Am J Public Health 1991;811498- 1505PubMedGoogle ScholarCrossref
Rosen  G The case of the consumptive conductor, or public health on a streetcar: a centennial tribute to Alfred F. Hess, MD.  Am J Public Health 1975;65977- 978Google ScholarCrossref
Duffy  J A History of Public Health in New York City 1866-1966.  New York, NY Russell Sage Foundation1974;
Flexner  A Alfred Fabian Hess: biographical memoir. Hess  AF Collected Writings 1 Springfield, Ill Charles C Thomas1936;ix- xxviiiGoogle Scholar
Hess  AFFish  M Infantile scurvy: the blood, the blood-vessels and the diet.  AJDC 1914;8385- 405Google Scholar
Rajakumar  K Infantile scurvy: a historical perspective.  Pediatrics 2001;108e76Google ScholarCrossref
Hess  AFUnger  LJ The cure of infantile rickets by artificial light and sunlight.  JAMA 1921;7739- 41Google Scholar
Hess  AF The cure of infantile rickets by sunlight accompanied by an increase in the inorganic phosphate of the blood.  JAMA 1922;7829Reprinted in:Hess  AF Collected Writings 1 Springfield, Ill Charles C Thomas1936;676- 679Google ScholarCrossref