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.

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

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.

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.

The diagnostic and prognostic role of cerebrospinal fluid biomarkers in glucose transporter 1 deficiency: a systematic review.

Authors: Mastrangelo, Mario Manti, Filippo Ricciardi, Giacomina et al.

Source: European Journal of Pediatrics. Sep2024, Vol. 183 Issue 9, p3665-3678. 14p.

Removal notice to "An Egyptian patient with Schwartz-Jampel syndrome type I and new ocular findings" [Egypt J Med Hum Genet 18 (2017) 393-396].

Authors: Elsayed, Solaf M. Gamal, Radwa

Source: Egyptian Journal of Medical Human Genetics. Oct2018, Vol. 19 Issue 4, p443-443. 1p.

Diagnosis and management of patients with Gaucher disease: an Egyptian expert opinion.

Authors: El-Beshlawy, Amal Tantawy, Azza A. G. Shawky, Rabah M. et al.

Source: Egyptian Journal of Medical Human Genetics. 7/31/2024, Vol. 25 Issue 1, p1-16. 16p.

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.

Subclinical hypothyroidism in children with Down syndrome: To treat or not to treat???

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

Source: Egyptian Journal of Medical Human Genetics. 2014, Vol. 15 Issue 4, p407-408. 2p.

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.

Professor Rabah Mohamed Shawky, 1943-2021.

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

Source: Egyptian Journal of Medical Human Genetics. 8/20/2021, Vol. 22, p1-1. 1p.

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.

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.

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.