Search Results - "Elsayed, Solaf"

Study title: bone health in patients with isolated methylmalonic acidemia.

Authors: Elsayed, Solaf M. El Sedfy, Heba Hassan Omar, Omar Hussain et al.

Source: Egyptian Journal of Medical Human Genetics. 4/13/2026, Vol. 27 Issue 1, p1-8. 8p.

Correction: Bone health in patients with isolated methylmalonic acidemia.

Authors: Elsayed, Solaf M. El Sedfy, Heba Hassan Omar, Omar Hussain et al.

Source: Egyptian Journal of Medical Human Genetics. 5/11/2026, Vol. 27 Issue 1, p1-1. 1p.

A note of thanks.

Authors: Elsayed, Solaf¹ (AUTHOR) elsayed683@yahoo.com

Source: Egyptian Journal of Medical Human Genetics. 12/28/2021, Vol. 22 Issue 1, p1-5. 5p.

ADH1B, the adipocyte-enriched alcohol dehydrogenase, plays an essential, cell-autonomous role in human adipogenesis.

Authors: Gautheron, Jérémie Elsayed, Solaf Pistorio, Valeria et al.

Source: Proceedings of the National Academy of Sciences of the United States of America. 6/11/2024, Vol. 121 Issue 24, p1-9. 37p.

Subjects: Alcohol dehydrogenase, Human stem cells, Adipose tissues, Adipogenesis, Missense mutation

Metabolic and other morbid complications in congenital generalized lipodystrophy type 4.

Authors: Akinci, Gulcin Alyaarubi, Saif Patni, Nivedita et al.

Source: American Journal of Medical Genetics. Part A; Jun2024, Vol. 194 Issue 6, p1-15, 15p

An Egyptian patient with Schwartz-Jampel syndrome type I and new ocular findings.

Authors: Elsayed, Solaf M. Gamal, Radwa

Source: Egyptian Journal of Medical Human Genetics. 2017, Vol. 18 Issue 4, p393-396. 4p.

Treatment options for patients with Gaucher disease.

Authors: Shawky, Rabah M. Elsayed, Solaf M.

Source: Egyptian Journal of Medical Human Genetics. Jul2016, Vol. 17 Issue 3, p281-285. 5p.

Wolman disease in patients with familial hemophagocytic lymphohistiocytosis (FHL) negative mutations.

Authors: Elsayed, Solaf Elsobky, Ezzat Tantawy, Azza et al.

Source: Egyptian Journal of Medical Human Genetics. Jul2016, Vol. 17 Issue 3, p277-280. 4p.

Autosomal recessive ichthyosis with limb reduction defect: A simple association and not CHILD syndrome.

Authors: Shawky, Rabah M. Elsayed, Solaf M. Amgad, Heba

Source: Egyptian Journal of Medical Human Genetics. Jul2016, Vol. 17 Issue 3, p255-258. 4p.

Treatment-induced copper deficiency in two patients with Wilson’s disease.

Authors: Abdel Ghaffar, Tawhida Y. Elsayed, Solaf M. Naghi, Suzan E. l. et al.

Source: Egyptian Liver Journal. Jan-Oct2016, Vol. 6 Issue 1, p16-20. 5p. 3 Charts.

Non-deletion mutations in Egyptian patients with Duchenne muscular dystrophy.

Authors: Shawky, Rabah M. Elsayed, Solaf M. Todorov, Theodor et al.

Source: Egyptian Journal of Medical Human Genetics. 2014, Vol. 15 Issue 3, p235-240. 6p.

Maternal MTHFR C677T genotype and septal defects in offspring with Down syndrome: A pilot study.

Authors: Elsayed, Ghada M. Elsayed, Solaf M. Ezz-Elarab, Sahar S.

Source: Egyptian Journal of Medical Human Genetics. 2014, Vol. 15 Issue 1, p39-44. 6p.

Familial Peters Plus syndrome with absent anal canal, sacral agenesis and sensorineural hearing loss: Expanding the clinical spectrum.

Authors: Shawky, Rabah M. Elsayed, Solaf M. Abd-Elkhalek, Heba S. et al.

Source: Egyptian Journal of Medical Human Genetics. 2013, Vol. 14 Issue 4, p423-428. 6p.

Oral-facial-digital syndrome type II: Transitional type between Mohr and Varadi.

Authors: Shawky, Rabah M. Elsayed, Solaf M. Abd-Elkhalek, Heba S. et al.

Source: Egyptian Journal of Medical Human Genetics. 2013, Vol. 14 Issue 3, p311-315. 5p. 5 Color Photographs, 3 Black and White Photographs.

Consanguinity and its relevance to clinical genetics.

Authors: Shawky, Rabah M. Elsayed, Solaf M. Zaki, Mouchira E. et al.

Source: Egyptian Journal of Medical Human Genetics. 2013, Vol. 14 Issue 2, p157-164. 8p. 9 Charts.

Multiple pterygium syndrome with marked pterygia of the fingers and MRI changes in the spine.

Authors: Shawky, Rabah M. Elsayed, Solaf Gaboon, Nagwa

Source: Egyptian Journal of Medical Human Genetics. 2012, Vol. 13 Issue 1, p107-113. 7p. 7 Color Photographs, 3 Black and White Photographs.

Factor V G1691A (Leiden) is a major etiological factor in Egyptian Budd-Chiari syndrome patients.

Alternate Title: Mısır'lı Budd-Chiari sendromlu hastalarda Faktör G1691A Leiden major bir etyolojik faktördür.

Authors: Ghaffar, Tawhida Y. Abdel Elsayed, Solaf M. Sakr, Mohamed A. et al.

Source: Turkish Journal of Hematology. Dec2011, p299-305. 7p.

Educational corner of the issue.

Authors: Elsayed, Solaf M.¹ elsayed683@yahoo.com

Source: Egyptian Journal of Medical Human Genetics. 2011, Vol. 12 Issue 2, p221-224. 4p.

Therapeutic approaches to genetic disorders.

Authors: Zaghloul, Mohammad S. Elsayed, Solaf M. Hosseny, Heba Alla A.

Source: Egyptian Journal of Medical Human Genetics. 2009, Vol. 10 Issue 2, p118-128. 11p. 1 Diagram, 2 Charts.

Triple A syndrome presenting with myopathy: An Egyptian patient.

Authors: Shawky, Rabah M. Elsayed, Solaf M. Elsedfy, Heba H.

Source: Egyptian Journal of Medical Human Genetics. 2009, Vol. 10 Issue 1, p105-109. 5p. 2 Color Photographs.