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Epilepsy & Behavior : E&B
|
February 24, 2009
Two new familial severe infantile spasm syndromes in males
Pascale E Karam, Chantal Farra, Alhan Shamseddine, et al.
Genes
|
February 27, 2026
Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
Rima Hanna-Wakim, Pascale E Karam, Mazen Kurban, et al.
Metabolic Brain Disease
|
June 4, 2024
Hyperornithinemia-hyperammonemia-homocitrullinuria: a rare neurometabolic disorder in two siblings
Diane Rizkallah, Rose T Daher, Laith Haddad, et al.
IEEE Transactions on Bio-Medical Engineering
|
July 1, 1993
Mechanics of the occlusive arm cuff and its application as a volume sensor
G Drzewiecki, V Bansal, E Karam, et al.
Clinical Medicine Insights. Pediatrics
|
August 14, 2025
The Diagnostic Saga of a Rare Congenital Bile Acid Synthesis Disorder: A Case Report
Nadine Yazbeck, Rima Hanna-Wakim, Dolly Noun, et al.
Neuropediatrics
|
March 19, 2009
Biotin-responsive basal ganglia disease: case report and review of the literature
T I El-Hajj, P E Karam, M A Mikati
Gene
|
December 11, 2012
Spectrum of mutations in Lebanese patients with phenylalanine hydroxylase deficiency
Pascale E Karam, Rasha Shahabeddeen Alhamra, Georges Nemer, et al.
Frontiers in Pediatrics
|
August 23, 2021
Diagnostic and Therapeutic Challenges of Hereditary Tyrosinemia Type 1 in Lebanon: A 12-Year Retrospective Review
Karim N Daou, Abir Barhoumi, Amina Bassyouni, et al.
Attachment & Human Development
|
October 4, 2024
Father-separation and well-being in forcibly displaced Syrian children
H Eltanamly, A May, F McEwen, et al.
The Journal of Rheumatology
|
October 1, 1994
Rheumatoid nodulosis of the meninges
N E Karam, L Roger, L L Hankins, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 84) with videos related to
Sort By:
Page
of 9
Epilepsy & Behavior : E&B
|
February 24, 2009
Two new familial severe infantile spasm syndromes in males
Pascale E Karam, Chantal Farra, Alhan Shamseddine, et al.
Genes
|
February 27, 2026
Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
Rima Hanna-Wakim, Pascale E Karam, Mazen Kurban, et al.
Metabolic Brain Disease
|
June 4, 2024
Hyperornithinemia-hyperammonemia-homocitrullinuria: a rare neurometabolic disorder in two siblings
Diane Rizkallah, Rose T Daher, Laith Haddad, et al.
IEEE Transactions on Bio-Medical Engineering
|
July 1, 1993
Mechanics of the occlusive arm cuff and its application as a volume sensor
G Drzewiecki, V Bansal, E Karam, et al.
Clinical Medicine Insights. Pediatrics
|
August 14, 2025
The Diagnostic Saga of a Rare Congenital Bile Acid Synthesis Disorder: A Case Report
Nadine Yazbeck, Rima Hanna-Wakim, Dolly Noun, et al.
Neuropediatrics
|
March 19, 2009
Biotin-responsive basal ganglia disease: case report and review of the literature
T I El-Hajj, P E Karam, M A Mikati
Gene
|
December 11, 2012
Spectrum of mutations in Lebanese patients with phenylalanine hydroxylase deficiency
Pascale E Karam, Rasha Shahabeddeen Alhamra, Georges Nemer, et al.
Frontiers in Pediatrics
|
August 23, 2021
Diagnostic and Therapeutic Challenges of Hereditary Tyrosinemia Type 1 in Lebanon: A 12-Year Retrospective Review
Karim N Daou, Abir Barhoumi, Amina Bassyouni, et al.
Attachment & Human Development
|
October 4, 2024
Father-separation and well-being in forcibly displaced Syrian children
H Eltanamly, A May, F McEwen, et al.
The Journal of Rheumatology
|
October 1, 1994
Rheumatoid nodulosis of the meninges
N E Karam, L Roger, L L Hankins, et al.
Page
of 9