Solaf M. Elsayed
Cairo, C, Egypt
Last Updated: 09/26/2026
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Found 27 publications
European Consortium for Lipodystrophies consensus definition and classification framework for monogenic lipodystrophy.
Journal: Journal of internal medicine
Published: September 02, 2026
Clinical and molecular characteristics of fructose 1, 6 bisphosphatase deficiency in 6 Egyptian patients and two common variants.
Journal: Orphanet journal of rare diseases
Published: March 19, 2025
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.
Journal: Molecular and cellular pediatrics
Published: February 15, 2025
ADH1B, the adipocyte-enriched alcohol dehydrogenase, plays an essential, cell-autonomous role in human adipogenesis.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: June 05, 2024
Hemophagocytic lymphohistiocytosis in Egyptian children: diagnosis, treatment challenges, and outcome.
Journal: Expert review of hematology
Published: April 10, 2024
Metabolic and other morbid complications in congenital generalized lipodystrophy type 4.
Journal: American journal of medical genetics. Part A
Published: October 08, 2023
A cross-sectional analysis of the association between diabetes self-care practices and blood glucose regulation among Egyptian diabetic patients.
Journal: European review for medical and pharmacological sciences
Published: July 17, 2023
Extra-hepatic portal vein thrombosis in children: Single center experience.
Journal: Clinical and experimental hepatology
Published: December 24, 2022
An integrated multiomic approach as an excellent tool for the diagnosis of metabolic diseases: our first 3720 patients.
Journal: European journal of human genetics : EJHG
Published: February 16, 2022
Skeletal radiology following hematopoietic stem cell transplantation in infantile osteopetrosis: an overlooked assessment tool.
Journal: Boletin medico del Hospital Infantil de Mexico
Published: July 27, 2021
Multicentric Osteolysis, Nodulosis, and Arthropathy in two unrelated children with matrix metalloproteinase 2 variants: Genetic-skeletal correlations.
Journal: Bone reports
Published: June 10, 2021
Last Updated: 09/26/2026