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Wiskott-Aldrich syndrome with normal platelet volume in a low-income setting: a case report.
Ther Adv Rare Dis. 2021 Apr 26;2:26330040211009905. doi: 10.1177/26330040211009905. eCollection 2021 Jan-Dec.
Ther Adv Rare Dis. 2021.
PMID: 37181115
Free PMC article.
Factor VII deficiency: a rare genetic bleeding disorder in a 7-year-old child: a case report.
Salum HM, Lukumay J, Muze K, Swai P, Kindole C, Kipasika H, Apollo M, Chirande L, Furia F.
Salum HM, et al.
J Med Case Rep. 2023 Apr 14;17(1):138. doi: 10.1186/s13256-023-03884-3.
J Med Case Rep. 2023.
PMID: 37055867
Free PMC article.
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A ten year review of the sickle cell program in Muhimbili National Hospital, Tanzania.
Makani J, Tluway F, Makubi A, Soka D, Nkya S, Sangeda R, Mgaya J, Rwezaula S, Kirkham FJ, Kindole C, Osati E, Meda E, Snow RW, Newton CR, Roberts D, Aboud M, Thein SL, Cox SE, Luzzatto L, Mmbando BP.
Makani J, et al.
BMC Hematol. 2018 Nov 14;18:33. doi: 10.1186/s12878-018-0125-0. eCollection 2018.
BMC Hematol. 2018.
PMID: 30459954
Free PMC article.
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Severe congenital neutropenia with elastase, neutrophil expressed (ELANE) gene mutation in a Tanzanian child.
Shoo A, Swai P, Kindole C, Ngailo E, Godfrey E, Massawe E, Warren AJ, Luzzatto L.
Shoo A, et al.
Br J Haematol. 2022 Mar;196(5):1271-1274. doi: 10.1111/bjh.17924. Epub 2021 Nov 1.
Br J Haematol. 2022.
PMID: 34725814
No abstract available.
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