Zobrazeno 1 - 10
of 53
pro vyhledávání: '"A. Babakhoya"'
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
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
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
Autor:
Soulaimane, M'harzi, Elouali, Aziza, Najioui, Younesse, Ghanam, Ayad, Rkain, Maria, Babakhoya, Abdeladim, Lamalmi, Najat, Bennani, Amal, Benajiba, Noufissa
Publikováno v:
In Journal of Clinical and Translational Endocrinology: Case Reports June 2022 24
Publikováno v:
Archives de Pédiatrie. 21:214-218
The clinical aspects of neonatal cerebral venous thrombosis are polymorphic in their mode of onset, making diagnosis difficult. Transfontanellar ultrasound allows for the morphological and vascular exploration of intracranial contents. We report thre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10cdfd88f0b826e41e046f3a6a08bbcc
https://doi.org/10.1016/j.arcped.2013.11.012
https://doi.org/10.1016/j.arcped.2013.11.012