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D S Hummell

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Archives of Pediatrics & Adolescent Medicine|July 13, 2000
Scurvy presenting as painful gait with bruising in a young boyY Tamura, D C Welch, J A Zic, et al.
Journal of Clinical Immunology|November 1, 1994
Increased interleukin-6 (IL-6) production in a young child with clinical and pathologic features of multicentric Castleman's diseaseM C Kinney, D S Hummell, P M Villiger, et al.
The Journal of Infectious Diseases|April 1, 1987
Meningitis caused by a nonencapsulated strain of Neisseria meningitidis in twin infants with a C6 deficiencyD S Hummell, L F Mocca, C E Frasch, et al.
The Journal of Pediatrics|February 21, 1998
Complete DiGeorge syndrome: persistence of profound immunodeficiencyM L Markert, D S Hummell, H M Rosenblatt, et al.
The Journal of Clinical Investigation|November 1, 1993
Novel splicing, missense, and deletion mutations in seven adenosine deaminase-deficient patients with late/delayed onset of combined immunodeficiency disease. Contribution of genotype to phenotypeI Santisteban, F X Arredondo-Vega, S Kelly, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Archives of Pediatrics & Adolescent Medicine|July 13, 2000
Scurvy presenting as painful gait with bruising in a young boyY Tamura, D C Welch, J A Zic, et al.
Journal of Clinical Immunology|November 1, 1994
Increased interleukin-6 (IL-6) production in a young child with clinical and pathologic features of multicentric Castleman's diseaseM C Kinney, D S Hummell, P M Villiger, et al.
The Journal of Infectious Diseases|April 1, 1987
Meningitis caused by a nonencapsulated strain of Neisseria meningitidis in twin infants with a C6 deficiencyD S Hummell, L F Mocca, C E Frasch, et al.
The Journal of Pediatrics|February 21, 1998
Complete DiGeorge syndrome: persistence of profound immunodeficiencyM L Markert, D S Hummell, H M Rosenblatt, et al.
The Journal of Clinical Investigation|November 1, 1993
Novel splicing, missense, and deletion mutations in seven adenosine deaminase-deficient patients with late/delayed onset of combined immunodeficiency disease. Contribution of genotype to phenotypeI Santisteban, F X Arredondo-Vega, S Kelly, et al.
Pageof 2