Literature DB >> 2642320

Herrick's 1910 case report of sickle cell anemia. The rest of the story.

T L Savitt1, M F Goldberg.   

Abstract

James B. Herrick's 1910 article presenting the case of an anemic West Indian student with peculiar-shaped red blood cells was the first description of sickle cell anemia in Western medical literature. However, he told only part of the story. Records in Chicago, Washington, DC, and Grenada, West Indies, reveal more information about the events surrounding Herrick's discovery and help put them in historical perspective. Herrick's intern, Ernest E. Irons, abreast of the latest developments in medicine, actually performed the blood work and alerted Herrick about the odd-looking cells. Changing patterns in American race relations allowed the patient, Walter Clement Noel, to study dentistry in Chicago. He continued to receive care from Irons for 2 1/2 years, then returned to Grenada to practice dentistry. Noel died nine years after his return to Grenada, at age 32.

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Year:  1989        PMID: 2642320

Source DB:  PubMed          Journal:  JAMA        ISSN: 0098-7484            Impact factor:   56.272


  10 in total

1.  Vascular risk assessment in patients with sickle cell disease.

Authors:  Claudia R Morris
Journal:  Haematologica       Date:  2011-01       Impact factor: 9.941

Review 2.  Gene therapy for sickle cell disease: An update.

Authors:  Selami Demirci; Naoya Uchida; John F Tisdale
Journal:  Cytotherapy       Date:  2018-05-30       Impact factor: 5.414

Review 3.  Advances in sickle cell therapies in the hydroxyurea era.

Authors:  Joshua J Field; David G Nathan
Journal:  Mol Med       Date:  2014-12-16       Impact factor: 6.354

4.  Double-blind, randomized, multicenter phase 2 study of SC411 in children with sickle cell disease (SCOT trial).

Authors:  Ahmed A Daak; Carlton D Dampier; Beng Fuh; Julie Kanter; Ofelia A Alvarez; L Vandy Black; Melissa A McNaull; Michael U Callaghan; Alex George; Lynne Neumayr; Lee M Hilliard; Fredrick Sancilio; Adrian L Rabinowicz; Matthew M Heeney
Journal:  Blood Adv       Date:  2018-08-14

Review 5.  Pediatric sickle cell disease: past successes and future challenges.

Authors:  Emily Riehm Meier; Angeli Rampersad
Journal:  Pediatr Res       Date:  2016-10-05       Impact factor: 3.756

6.  Bioinformatic primer for clinical and translational science.

Authors:  Randolph S Faustino; Anca Chiriac; Andre Terzic
Journal:  Clin Transl Sci       Date:  2008-09       Impact factor: 4.689

7.  Sickle cell disease: More than a century of progress. Where do we stand now?

Authors:  Valentine Brousse; David C Rees
Journal:  Indian J Med Res       Date:  2021-07       Impact factor: 2.375

8.  Analyzing Effects of Sickle Cell Disease on Morphometric and Cranial Growth in Indian Population.

Authors:  Kumari Menka; Kumar Anand; Mrigank Shekhar Jha; Abhinav Goel; Saba Nasreen; Devendra H Palve
Journal:  J Pharm Bioallied Sci       Date:  2021-11-10

Review 9.  Sickle Cell Disease in Children and Adolescents: A Review of the Historical, Clinical, and Public Health Perspective of Sub-Saharan Africa and Beyond.

Authors:  Walufu Ivan Egesa; Gloria Nakalema; William M Waibi; Munanura Turyasiima; Emmanuel Amuje; Gloria Kiconco; Simon Odoch; Patrick Kumbowi Kumbakulu; Said Abdirashid; Daniel Asiimwe
Journal:  Int J Pediatr       Date:  2022-10-08

10.  mTOR Inhibition improves anaemia and reduces organ damage in a murine model of sickle cell disease.

Authors:  Jintao Wang; Jennifer Tran; Hui Wang; Chiao Guo; David Harro; Andrew D Campbell; Daniel T Eitzman
Journal:  Br J Haematol       Date:  2016-03-31       Impact factor: 8.615

  10 in total

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