Zobrazeno 1 - 10
of 59
pro vyhledávání: '"A. Babakhoya"'
Autor:
M'harzi Soulaimane, Aziza Elouali, Younesse Najioui, Ayad Ghanam, Maria Rkain, Abdeladim Babakhoya, Najat Lamalmi, Amal Bennani, Noufissa Benajiba
Publikováno v:
Journal of Clinical and Translational Endocrinology Case Reports, Vol 24, Iss , Pp 100111- (2022)
Unbalanced diabetes can lead to many complications related to insulin deficiency. Hepatocytic glycogenic overload, formerly known as Mauriac syndrome, is one of them. It is a rare syndrome initially described in children with type 1 diabetes (T1D) wh
Externí odkaz:
https://doaj.org/article/311deb970bb8434dbc0f4b838187050a
Publikováno v:
OALib. 10:1-6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8ed2d77458a910acae7575522314f01
https://doi.org/10.4236/oalib.1110019
https://doi.org/10.4236/oalib.1110019
Publikováno v:
Rheumatology. 61
Introduction Juvenile Idiopathic Arthritis (JIA) is a group of conditions in which the first sign of the disease appears before the child's 16th birthday. The common feature is the presence of at least one arthritis of > 6 weeks’ duration with no r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4db178102a32fe50eb56608385f2d08
https://doi.org/10.1093/rheumatology/keac495.003
https://doi.org/10.1093/rheumatology/keac495.003
Publikováno v:
Rheumatology. 60
Background Takayasu's arteritis (TA) is a chronic inflammatory vasculitis of unknown origin. It affects the large vessels, especially the aorta, its main branches, and the pulmonary arteries. It begins acutely in children with severe general manifest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c90060f28f226a07b71fad7ccaae973d
https://doi.org/10.1093/rheumatology/keab722.080
https://doi.org/10.1093/rheumatology/keab722.080
Autor:
Mounia Lakhdar Idrissi, Abdeladim Babakhoya, Kawtar Khabbache, Fatimzohra Souilmi, Sara Benmiloud, Sanae Abourrazak, Sanae Chaouki, Samir Atmani, Abdelhak Bouharrou, Moustapha Hida
Publikováno v:
The Pan African Medical Journal, Vol 14, Iss 6 (2013)
La maladie de Wilson ou dégénérescence hépato-lenticulaire est une affection génétique autosomique récessive caractérisée par une accumulation toxique de cuivre dans l'organisme, essentiellement dans le foie, le système nerveux central et l
Externí odkaz:
https://doaj.org/article/6e8e2be9ee3d4a8d8ae1f88a3a8ade3f
Publikováno v:
The Pan African Medical Journal, Vol 12, Iss 51 (2012)
INTRODUCTION: L'hypertension portale n'est pas exceptionnelle chez l'enfant. L'hémorragie digestive en est une complication redoutable pouvant mettre en jeu le pronostic vital. Cette hémorragie, pouvant être isolée, confie à l'examen endoscopiqu
Externí odkaz:
https://doaj.org/article/876e59d2d62044b4981aec2fca860a1a
Autor:
Mustapha El Kouache, S. Labib, A. El Madi, A. Babakhoya, S. Atmani, Y. Abouabdilah, M. Harandou
Publikováno v:
Case Reports in Cardiology, Vol 2012 (2012)
Cantrell syndrome is a very rare congenital disease associating five features: a midline, upper abdominal wall disorder, lower sternal abnormality, anterior diaphragmatic defect, diaphragmatic pericardial abnormality, and congenital abnormalities of
Externí odkaz:
https://doaj.org/article/97dbbc01578c454093abd0cc89698e47
Publikováno v:
The Pan African Medical Journal, Vol 10, Iss 51 (2011)
Le syndrome de Currarino (SC) est defini par une triade rassemblant une malformation ano-rectale, une agenesie sacree et une tumeur pre-sacree. Nous rapportons le cas d�une fille de 4 ans et demi ayant ete admise en consultation de gastro-enterolog
Externí odkaz:
https://doaj.org/article/9aae60f9198c42fab725d0aac2fa4ed5
Publikováno v:
African Journal of Paediatric Surgery, Vol 10, Iss 2, Pp 199-200 (2013)
The finding of a double-chambered right ventricle (DCRV) is exceptionally rare as an isolated anomaly. It is a congenital cardiac anomaly in which the right ventricle is separated into two chambers, a proximal high-pressure chamber and a distal low-p
Externí odkaz:
https://doaj.org/article/71c5046aa1d541d1a3e3b0cfd368bbbc
Autor:
Idrissi, Mounia Lakhdar1, Babakhoya, Abdeladim1, Khabbache, Kawtar1, Souilmi, Fatimzohra1, Benmiloud, Sara1, Abourrazak, Sanae1, Chaouki, Sanae1, Atmani, Samir1, Bouharrou, Abdelhak1, Hida, Moustapha1
Publikováno v:
Pan African Medical Journal. 2013, Vol. 14, p1-6. 6p.