Výsledky vyhledávání - "Daniel Mahfoud"

Report on a Case with Moreno-Nishimura-Schmidt Overgrowth Syndrome: A Clinically Delineated Disease Yet of an Unknown Origin!

Autor: Cybel Mehawej, Eliane Chouery, Ghada Al Hage Chehade, Yosra Bejaoui, Daniel Mahfoud, Maya Gerges, Valérie Delague, Nady El Hajj, Andre Megarbane

Publikováno v: Molecular Syndromology. :1-6

Introduction: Overgrowth syndromes are a heterogeneous group of genetic disorders characterized by excessive growth, often accompanied by additional clinical features, such as facial dysmorphism, hormonal imbalances, cognitive impairment, and increas

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4ebf8e6fea0b1d5da4027a335b05e1fd
https://doi.org/10.1159/000527215

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Hepatic portal venous gas in the setting of closed loop small bowel obstruction in a patient with adjustable gastric band: a case report

Autor: Mandy Nakhle, Samer Diab, Nadim Kassir, Pamela Semaan, Rajaa Chatila, Daniel Mahfoud, Georges Al-Hajj, Rodrigue Chemaly

Publikováno v: European Journal of Medical Case Reports. :60-64

Background: Hepatic portal venous gas (HPVG) has rarely been described in the presence of benign, non-life-threatening conditions such as gastric emphysema and gastric dilatation. In such cases, management and patient prognosis have evolved to become

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ea6df8a80758abbb1583691193cf34e2
https://doi.org/10.24911/ejmcr/173-1662991450

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Spondyloocular Syndrome: A Report of an Additional Family and Phenotypic Spectrum Delineation

Autor: Eliane Chouery, Rim Karam, Yves Najm Mrad, Cybel Mehawej, Nahia Dib El Jalbout, Jamal Bleik, Daniel Mahfoud, Andre Megarbane

Publikováno v: Genes. 14:497

Spondyloocular syndrome (SOS, OMIM # 605822) is a rare genetic disorder characterized by osseous and ocular manifestations, including generalized osteoporosis, multiple long bones fractures, platyspondyly, dense cataracts and retinal detachment, and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9906c27caeeee6f9211407ff6a54aa60
https://doi.org/10.3390/genes14020497

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Clinical and Molecular Update on the Fourth Reported Family with Hamamy Syndrome

Autor: Christel Dagher, Audrey Criqui, Nathalie Roeckel-Trevisiol, Christel Castro, Daniel Mahfoud, Hala Mégarbané, Sylvain Baulande, André Mégarbané, Sayeeda Hana, Stephany El-Hayek, Mahmoud Taleb Al-Ali, Jean-Pierre Desvignes, Valérie Delague

Publikováno v: Molecular Syndromology
Molecular Syndromology, 2021, 12 (6), pp.342-350. ⟨10.1159/000517253⟩
Mol Syndromol
Molecular Syndromology, Karger, 2021, 12 (6), pp.342-350. ⟨10.1159/000517253⟩

We report on 2 cousins, a girl and a boy, born to first-cousin Lebanese parents with Hamamy syndrome, exhibiting developmental delay, intellectual disability, severe telecanthus, abnormal ears, dentinogenesis imperfecta, and bone fragility. Whole-exo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fd26fd4373b9c4259fcbc827655ef5b
https://hal-amu.archives-ouvertes.fr/hal-03662760

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Radiology residents from learners to teachers: A multi-centric study

Autor: Roy A. Raad, Andrew Barakat, Zeina Farah, Ghida Saheb, Daniel Mahfoud, Fady Haddad, Amro Baassiri, Lara Nassar

Publikováno v: European journal of radiology. 134

Purpose The teaching role of radiology residents has seldom been evaluated, and little is known about how teaching skills of radiology residents evolve throughout their training in the absence of formal teaching guidance. Our objective is to identify

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c028ae4e566d034786f8ef948a423b45
https://pubmed.ncbi.nlm.nih.gov/33290976

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Disseminated Intra-Abdominal Aspergilloma With Abdominal Wall Invasion in a Patient With Acute Myeloid Leukemia: A Case Report

Autor: Hady Ghanem, Georges Khoury, Linda Rached, Daniel Mahfoud, Marie-Therezia Hadchiti, Mohamad Abdalkader

Publikováno v: Clinical Lymphoma Myeloma and Leukemia. 15:S94-S97

Invasive aspergillosis represents a major cause of morbidity and mortality in immunocompromised patients. Involvement of the gastrointestinal (GI) tract by Aspergillus infection is mostly reported as part of a disseminated infection from a primary pu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ffe7648afc5554706392b53c22b3c3d
https://doi.org/10.1016/j.clml.2014.12.017

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Budd-Chiari syndrome and heparin-induced thrombocytopenia in polycythemia vera: Successful treatment with repeated TIPS and interferon alpha

Autor: Nathalie Mahfoud, Daniel Mahfoud, Riad Akoum, Albert Ghaoui, Nadine Haddad, Hussein Farhat, Joe Khoury

Publikováno v: Journal of Cancer Research and Therapeutics, Vol 5, Iss 4, Pp 305-308 (2009)

Polycythemia vera (PV) is a common cause of Budd-Chiari syndrome (BCS) and portal vein thrombosis (PVT). The postpartum period is a precipitating cofactor. An additional heparin-induced thrombocytopenia/thrombosis (HIT/T) leads to a life-threatening

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::279adbb03d57e0c8df43d306a513b72d
https://doi.org/10.4103/0973-1482.59917

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