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Hala Abi Rached Megarbane

Observed names: H Mégarbané, H. Abi‐Rached Mégarbané, H. Megarbane, H. Mégarbané, Hala A Megarbane, Hala Megarbane, Hala Mégarbané, Megarbane Hala Abi Rached, Mégarbané, Hala
Observed institutions: Hôpital Necker-Enfants Malades, University of Balamand, Saint Joseph University, Saint George Hospital, Institut Necker Enfants Malades, Hôtel-Dieu de France, Hôpital Tenon, Université Pierre-et-Marie-Curie, American University of Beirut
ORCID: 0009-0005-0157-9952
Observed ORCID: 0009-0005-0157-9952
OpenAlex ID: A5112671524
Mutation in WNT10A Is Associated with an Autosomal Recessive Ectodermal Dysplasia: The Odonto-onycho-dermal Dysplasia
2007 · Lynn Adaimy, Eliane Chouery, et al. · The American Journal of Human Genetics · 249
Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
2011 · Hala Mégarbané, André Mégarbané · Orphanet Journal of Rare Diseases · 77
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Homozygous mutation of the IGF1 receptor gene in a patient with severe pre- and postnatal growth failure and congenital malformations
2012 · Marie-Hélène Gannagé-Yared, Jürgen Klammt, et al. · European Journal of Endocrinology · 63
A p.C217R Mutation in Fibulin-5 from Cutis Laxa Patients Is Associated with Incomplete Extracellular Matrix Formation in a Skin Equivalent Model
2008 · Stephanie Claus, Judith Fischer, et al. · Journal of Investigative Dermatology · 62
Ocular findings in ichthyosis follicularis-alopecia-photophobia (IFAP) syndrome
2004 · Elias Traboulsi, Naji Waked, et al. · Ophthalmic Genetics · 41
Genotype-Phenotype Correlations Emerging from the Identification of Missense Mutations inMBTPS2
2013 · Dorothea Bornholdt, T. Prescott Atkinson, et al. · Human Mutation · 40
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Contribution of next generation sequencing in pediatric practice in Lebanon. A Study on 213 cases
2018 · Pratibha Nair, Sandra Sabbagh, et al. · Molecular Genetics & Genomic Medicine · 35
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Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome: Report of a new family with additional features and review
2003 · Hala Mégarbané, Cynthia Zablit, et al. · American Journal of Medical Genetics Part A · 34
Unusual presentation of a severe autosomal recessive anhydrotic ectodermal dysplasia with a novel mutation in the EDAR gene
2008 · Hala Mégarbané, Céline Cluzeau, et al. · American Journal of Medical Genetics Part A · 33
Further delineation of the odonto–onycho–dermal dysplasia syndrome
2004 · Hala Mégarbané, May Haddad, et al. · American Journal of Medical Genetics Part A · 33
Congenital Erythropoietic Porphyria: Report of a Novel Mutation with Absence of Clinical Manifestations in a Homozygous Mutant Sibling
2004 · Cécile Ged, Hala Mégarbané, et al. · Journal of Investigative Dermatology · 30
Two Observations Raising Questions about Risk Factors of Cutaneous Necrosis Induced by Terlipressin (Glypressin®)
2009 · Hala Mégarbané, Stéphane Barete, et al. · Dermatology · 29
An Autosomal-Recessive Form of Cutis Laxa Is Due to Homozygous Elastin Mutations, and the Phenotype May Be Modified by a Heterozygous Fibulin 5 Polymorphism
2009 · Hala Mégarbané, Jobard Florence, et al. · Journal of Investigative Dermatology · 28
Neonatal Rhabdomyosarcoma Misdiagnosed as a Congenital Hemangioma
2010 · Hala Megarbane, Francois Doz, et al. · Pediatric Dermatology · 21
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Temporary henna tattoos and hypertrichosis: a case report and review of the literature
2015 · Constantin El Habr, Hala Mégarbané · Journal of Dermatological Case Reports · 17
Pediatric discoid lupus erythematosus: Short report
2021 · Tatiana Hawat, Salwa Ballouz, et al. · Dermatologic Therapy · 15
X-linked reticulate pigmentary layer. Report of a new patient and demonstration of a skewed X-inactivation.
2005 · H Mégarbané, N Boehm, et al. · PubMed · 13
Craniosynostosis, anal anomalies, and porokeratosis (CDAGS syndrome): Case report and literature review
2013 · Eliane Chouery, Claire Guissart, et al. · European Journal of Medical Genetics · 10
New autosomal recessive syndrome with short stature and facio–auriculo–thoracic malformations
2004 · André Mégarbané, Linda Daou, et al. · American Journal of Medical Genetics Part A · 7
Clinical and Molecular Update on the Fourth Reported Family with Hamamy Syndrome
2021 · André Mégarbané, Sayeeda Hana, et al. · Molecular Syndromology · 6
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Triple therapy approach for treating chromoblastomycosis in a Lebanese patient
2024 · Joe Khodeir, Paul Ohanian, et al. · Clinical Case Reports · 4
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Pseudoepitheliomatous keratotic and micaceous balanitis: A literature review
2021 · Antoine Salloum, Nagham Bazzi, et al. · Australasian Journal of Dermatology · 4
Don't miss this blue toe: Hair tourniquet syndrome
2014 · J. El‐Kehdy, J. Nasr, et al. · Journal of the European Academy of Dermatology and Venereology · 4
Pseudoepitheliomatous Keratotic and Micaceous Balanitis: A Distinct Entity
2021 · Antoine Salloum, Julien Bachour, et al. · Indian Journal of Dermatopathology and Diagnostic Dermatology · 3
Erythrodermie congénitale desquamative
2004 · H. Mégarbané, R. Tomb, et al. · Annales de Dermatologie et de Vénéréologie · 3
Works count: 37
Citation count: 864
H-index: 15
I10-index: 18
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