Publications by authors named "Solaf Elsayed"

Claim this Profile
C
Clinical and molecular characteristics of fructose 1, 6 bisphosphatase deficiency in 6 Egyptian patients and two common variants.
Solaf M Elsayed, Radwa G Mahmoud, Yasmeen Abdelaziz Fereig

Orphanet J Rare Dis· November 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Acid β-glucosidase (GBA1) gene mutational spectrum and clinical phenotypes in patients with gaucher disease: seven novel mutations in a multicenter retrospective cohort study from upper Egypt.
Mervat A M Youssef, Solaf M Elsayed, Khalid I Elsayh, Sherin A Taha, Hala S M Abdelmotogaly

Mol Cell Pediatr· October 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Metabolic and other morbid complications in congenital generalized lipodystrophy type 4.
Gulcin Akinci, Saif Alyaarubi, Nivedita Patni, Nadia Alhashmi, Azza Al-Shidhani, Solaf M Elsayed

Am J Med Genet A· June 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
ADH1B, the adipocyte-enriched alcohol dehydrogenase, plays an essential, cell-autonomous role in human adipogenesis.
Jérémie Gautheron, Solaf Elsayed, Valeria Pistorio, Sam Lockhart, Jamila Zammouri

Proc Natl Acad Sci U S A· June 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Hemophagocytic lymphohistiocytosis in Egyptian children: diagnosis, treatment challenges, and outcome.
Azza A Tantawy, Nayera H K Elsherif, Solaf M Elsayed, Heba G A Ali, Sara M Makkeyah

Expert Rev Hematol· May 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel mutation in two Chanarin Dorfman siblings with severe and heterogeneous clinical phenotype.
Solaf Mohamed Elsayed, Enza Torre, Daniela Tavian, Laura Moro, Corrado Angelini

Genes Dis· May 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Extra-hepatic portal vein thrombosis in children: Single center experience.
Tawhida Yassin Abdel-Ghaffar, Haidy Mohammed Zakaria, Suzan El Naghi, Solaf M Elsayed, Alaa Haseeb

Clin Exp Hepatol· March 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
An integrated multiomic approach as an excellent tool for the diagnosis of metabolic diseases: our first 3720 patients.
Ligia S Almeida, Catarina Pereira, Ruxandra Aanicai, Sabine Schröder, Tomasz Bochinski, Solaf M Elsayed

Eur J Hum Genet· September 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Disentangling molecular and clinical stratification patterns in beta-galactosidase deficiency.
Abdellah Tebani, Bénédicte Sudrié-Arnaud, Ivana Dabaj, Stéphanie Torre, Laur Domitille, Solaf Elsayed

J Med Genet· April 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Multicentric Osteolysis, Nodulosis, and Arthropathy in two unrelated children with matrix metalloproteinase 2 variants: Genetic-skeletal correlations.
Hanan Elsebaie, Mohamed Abdelhafiz Mansour, Solaf M Elsayed, Shady Mahmoud, Tamer A El-Sobky

Bone Rep· December 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Skeletal radiology following hematopoietic stem cell transplantation in infantile osteopetrosis: an overlooked assessment tool.
Tamer A El-Sobky, Solaf M Elsayed

Bol Med Hosp Infant Mex· July 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
MPI-CDG from a hepatic perspective: Report of two Egyptian cases and review of literature.
Tawhida Y Abdel Ghaffar, Bobby G Ng, Solaf M Elsayed, Suzan El Naghi, Sarah Helmy

JIMD Rep· November 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Frequency of inborn errors of metabolism screening for children with unexplained acute encephalopathy at an emergency department.
Mamdouh Abdel Maksoud, Solaf Mohamed ELsayed, Rania H Shatla, Abdulbasit Abdulhalim Imam, Riad M Elsayed

Neuropsychiatr Dis Treat· June 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read-through, and mutated in Heimler syndrome.
Christine Neuhaus, Tobias Eisenberger, Christian Decker, Sandra Nagl, Cornelia Blank, Solaf M Elsayed

Mol Genet Genomic Med· September 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Maladaptative Autophagy Impairs Adipose Function in Congenital Generalized Lipodystrophy due to Cavin-1 Deficiency.
Laurence Salle-Teyssières, Martine Auclair, Faraj Terro, Mona Nemani, Solaf M Elsayed

J Clin Endocrinol Metab· July 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutations in CDC45, Encoding an Essential Component of the Pre-initiation Complex, Cause Meier-Gorlin Syndrome and Craniosynostosis.
Aimee L Fenwick, Maciej Kliszczak, Fay Cooper, Jennie Murray, Luis Sanchez-Pulido, Solaf M Elsayed

Am J Hum Genet· July 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A case of infantile osteopetrosis: The radioclinical features with literature update.
Tamer Ahmed El-Sobky, Ezzat Elsobky, Ismaiel Sadek, Solaf M Elsayed, Mohamed Fawzy Khattab

Bone Rep· June 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The Cockayne Syndrome Natural History (CoSyNH) study: clinical findings in 102 individuals and recommendations for care.
Brian T Wilson, Zornitza Stark, Ruth E Sutton, Sumita Danda, Alka V Ekbote, Solaf M Elsayed

Genet Med· May 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
O
Orthopaedic manifestations of Proteus syndrome in a child with literature update.
Tamer Ahmed El-Sobky, Solaf M Elsayed, Dalia M E El Mikkawy

Bone Rep· December 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Non-manifesting AHI1 truncations indicate localized loss-of-function tolerance in a severe Mendelian disease gene.
Solaf M Elsayed, Jennifer B Phillips, Raoul Heller, Michaela Thoenes, Ezzat Elsobky

Hum Mol Genet· May 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Structural chromosomal abnormalities in couples with recurrent abortion in Egypt.
Nagwa E A Gaboon, Ahmed Ramy Mohamed, Solaf M Elsayed, Osama K Zaki, Mohamed A Elsayed

Turk J Med Sci· April 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Role of plasma amino acids and urinary organic acids in diagnosis of mitochondrial diseases in children.
Hamed M Shatla, Hoda Y Tomoum, Solaf M Elsayed, Iman A Elagouza, Rania H Shatla

Pediatr Neurol· December 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations.
Solaf M Elsayed, Raoul Heller, Michaela Thoenes, Maha S Zaki, Daniel Swan

Eur J Hum Genet· February 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Prominent extensor truncal dystonia in Egyptian patients with Wilson's disease.
Ali S Shalash, Solaf M Elsayed, Suzan Elnaghi, Susanne A Schneider, Tawhida Y Abdel Ghaffar

Mov Disord· January 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
TNF-α-308 G/A Polymorphism in Egyptian Budd-Chiari Syndrome Patients.
Yonca Eğin, Solaf Elsayed, Mohamed Sakr, Nejat Akar

Turk J Haematol· December 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis