Samira Sissaoui
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Explore the profile of Samira Sissaoui including associated specialties, affiliations and a list of published articles.
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10
Citations
77
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Recent Articles
1.
Hajji H, Imbard A, Spraul A, Taibi L, Barbier V, Habes D, et al.
Mol Genet Metab Rep
. 2022 Nov;
33:100933.
PMID: 36393896
Hereditary tyrosinemia type 1 (HT1) is a rare autosomal recessive disorder of phenylalanine and tyrosine catabolism due to a deficiency of fumarylacetoacetate hydrolase. HT1 has a large clinical spectrum with...
2.
Hukkinen M, Wong M, Demir Z, Hadj Salem R, Debray D, Renolleau S, et al.
J Pediatr Surg
. 2022 Jul;
57(11):666-675.
PMID: 35871859
Aims: After liver transplantation (LT), synthesis of coagulation factors by the graft recovers faster for pro thrombotic than anti thrombotic factors, resulting in a potential pro thrombotic imbalance. We studied...
3.
Benkirane M, Marelli C, Guissart C, Roubertie A, Ollagnon E, Choumert A, et al.
Genet Med
. 2021 Jul;
23(11):2160-2170.
PMID: 34234304
Purpose: Diagnosis of inherited ataxia and related diseases represents a real challenge given the tremendous heterogeneity and clinical overlap of the various causes. We evaluated the efficacy of molecular diagnosis...
4.
Defert C, Marret J, Lacaille F, Sissaoui S, Dupic L, Lardy H, et al.
J Pediatr Gastroenterol Nutr
. 2021 Apr;
73(1):e7-e10.
PMID: 33908741
Intractable ascites is a rare condition in children mainly caused by cirrhosis or lymphatic disorders. Internal drainage may be considered as rescue therapy. In our department, 4 patients ages from...
5.
Sissaoui S, Cochet M, Poinsot P, Bordat C, Collardeau-Frachon S, Lachaux A, et al.
J Pediatr Gastroenterol Nutr
. 2021 Apr;
73(1):4-8.
PMID: 33853111
Familial intestinal hypocholesterolemias, such as abetalipoproteinemia, hypobetalipoproteinemia, and chylomicron retention disease, are rare genetic diseases that result in a defect in the synthesis or secretion of lipoproteins containing apolipoprotein B.In...
6.
Brassier A, Krug P, Lacaille F, Pontoizeau C, Krid S, Sissaoui S, et al.
J Inherit Metab Dis
. 2019 Sep;
43(2):234-243.
PMID: 31525265
Organ transplantation is discussed in methylmalonic aciduria (MMA) for renal failure, and poor quality of life and neurological outcome. We retrospectively evaluated 23 French MMA patients after kidney (KT), liver-kidney...
7.
Nader E, Girard M, Leruez-Ville M, Sissaoui S, Lacaille F, Roque-Afonso A, et al.
Clin Res Hepatol Gastroenterol
. 2019 Jul;
44(2):174-180.
PMID: 31266724
Introduction: Hepatitis E virus (HEV) is a major cause of acute viral hepatitis worldwide, usually asymptomatic in children. However, a growing number of publications over the last decade have documented...
8.
Russell B, Whaley K, Bove K, Labilloy A, Lombardo R, Hopkin R, et al.
Hepatology
. 2019 Mar;
70(3):1066-1070.
PMID: 30912852
No abstract available.
9.
Fanna M, Baptiste A, Capito C, Ortego R, Pacifico R, Lesage F, et al.
Pediatr Transplant
. 2016 Sep;
20(8):1065-1071.
PMID: 27681842
This study analyzes the preoperative risk factors for intra-operative bleeding in our recent series of pediatric LTs. Between November 2009 and November 2014, 84 consecutive isolated pediatric LTs were performed...
10.
Nizery L, Chardot C, Sissaoui S, Capito C, Henrion-Caude A, Debray D, et al.
Clin Res Hepatol Gastroenterol
. 2016 Jan;
40(3):281-287.
PMID: 26775892
Biliary atresia (BA) is a rare and severe inflammatory and obliterative cholangiopathy that affects both extra- and intrahepatic bile ducts. BA symptoms occur shortly after birth with jaundice, pale stools...