Detalhe da pesquisa
1.
Deep venous thrombosis and acute pericarditis associated with severe acute respiratory syndrome coronavirus 2 infection in a Congolese infant with sickle cell disease: a case report.
J Med Case Rep
; 16(1): 307, 2022 Aug 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35945602
2.
Sacrococcygeal teratoma in a female newborn with clinical features of trisomy 13: a case report from Central Africa.
Int Med Case Rep J
; 8: 333-6, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26715863
3.
Fragile X syndrome with mosaic size mutation in a Bantu patient from Central Africa.
Clin Dysmorphol
; 27(2): 66-69, 2018 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-29319541
4.
[Change in serum albumin in protein-energety malnutrition in a Congolese urban-rural]. / Variation de l'albuminémie au cours de la malnutrition protéino-energétique dans une zone urbano-rurale congolaise.
Pan Afr Med J
; 20: 299, 2015.
Artigo
em Francês
| MEDLINE | ID: mdl-26161222
5.
[Hematological and nutritional profile of homozygous sickle cell SS aged 6 to 59 months in Lubumbashi, Democratic Republic of Congo]. / Profil hématologique et nutritionnel du drépanocytaire homozygote SS âgé de 6 à 59 mois à Lubumbashi, République Démocratique du Congo.
Pan Afr Med J
; 21: 276, 2015.
Artigo
em Francês
| MEDLINE | ID: mdl-26587126
6.
[Sickle cell disease in stationary phase in 6-59 months children in Lubumbashi: epidemiology and clinical features]. / Drépanocytose chez l'enfant lushois de 6 à 59 mois en phase stationnaire: épidémiologie et clinique.
Pan Afr Med J
; 19: 71, 2014.
Artigo
em Francês
| MEDLINE | ID: mdl-25709729
7.
[Association esophageal atresia type 3 - microcephaly: an incomplete Feingold syndrome?]. / Association atrésie de l'oesophage type 3 - microcéphalie: Un syndrome de Feingold incomplet?
Pan Afr Med J
; 13: 85, 2012.
Artigo
em Francês
| MEDLINE | ID: mdl-23396887
8.
[Congenital malformations in Lubumbashi (Democratic Republic of Congo): about 72 cases observed and advocacy for the development of a National Registry of Congenital Malformations and a National Reference Center for Human Genetics]. / Malformations congénitales à Lubumbashi (République Démocratique du Congo): à propos de 72 cas observés et plaidoyer en faveur du développement d'un Registre National des Malformations Congénitales et d'un Centre National de Référence de Génétique Humaine.
Pan Afr Med J
; 13: 84, 2012.
Artigo
em Francês
| MEDLINE | ID: mdl-23396951