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Solaf M. Elsayed

h-6 H-Index
141 Citations
18 Papers

Published Papers

18 indexed
1
Consanguinity and its relevance to clinical genetics
Egyptian Journal of Medical Human Genetics Q2 2013 10.1016/j.ejmhg.2013.01.002
94 citations 393
2
Treatment options for patients with Gaucher disease
Egyptian Journal of Medical Human Genetics Q2 2016 10.1016/j.ejmhg.2016.02.001
14 citations 391
3
Maternal MTHFR C677T genotype and septal defects in offspring with Down syndrome: A pilot study
Egyptian Journal of Medical Human Genetics Q2 2014 10.1016/j.ejmhg.2013.09.003
8 citations 382
4
Neurofibromatosis type 1 and multiple sclerosis: Genetically related diseases
Egyptian Journal of Medical Human Genetics Q2 2017 10.1016/j.ejmhg.2016.10.001
8 citations 387
5
Oral-facial-digital syndrome type II: Transitional type between Mohr and Varadi
Egyptian Journal of Medical Human Genetics Q2 2013 10.1016/j.ejmhg.2013.03.005
6 citations 390
6
Non-deletion mutations in Egyptian patients with Duchenne muscular dystrophy
Egyptian Journal of Medical Human Genetics Q2 2014 10.1016/j.ejmhg.2014.03.004
6 citations 383
7
Familial Peters Plus syndrome with absent anal canal, sacral agenesis and sensorineural hearing loss: Expanding the clinical spectrum
Egyptian Journal of Medical Human Genetics Q2 2013 10.1016/j.ejmhg.2013.05.005
2 citations 390
8
Treatment-induced copper deficiency in two patients with Wilson’s disease
Egyptian Liver Journal Q2 2016 10.1097/01.elx.0000481903.74931.f7
1 citations 387
9
BH4 deficiency with unusual presentations: Challenges and lessons
Egyptian Journal of Medical Human Genetics Q2 2016 10.1016/j.ejmhg.2015.10.003
1 citations 386
10
REMOVED: An Egyptian patient with Schwartz-Jampel syndrome type I and new ocular findings
Egyptian Journal of Medical Human Genetics Q2 2017 10.1016/j.ejmhg.2017.06.001
1 citations 390
11
A severe form of cholestasis lymphoedema syndrome (Aagenaes syndrome) with progressive arthritis
Egyptian Liver Journal Q2 2014 10.1097/01.elx.0000440957.91402.27
0 citations 386
12
Hypothyroidism could be the only manifestation of mitochondrial T8993C mutation in Leigh syndrome
Egyptian Journal of Medical Human Genetics Q2 2013 10.1016/j.ejmhg.2012.10.005
0 citations 381
13
The blessing effect of an extra copy of chromosome 21
Egyptian Journal of Medical Human Genetics Q2 2014 10.1016/j.ejmhg.2014.01.006
0 citations 383
14
Subclinical hypothyroidism in children with Down syndrome: To treat or not to treat???
Egyptian Journal of Medical Human Genetics Q2 2014 10.1016/j.ejmhg.2014.08.003
0 citations 382
15
Autosomal recessive ichthyosis with limb reduction defect: A simple association and not CHILD syndrome
Egyptian Journal of Medical Human Genetics Q2 2016 10.1016/j.ejmhg.2015.08.009
0 citations 385
16
Challenges in diagnosis and counseling of a family with two recessive neurometabolic disorders
Egyptian Journal of Medical Human Genetics Q2 2016 10.1016/j.ejmhg.2015.12.005
0 citations 389
17
Cardiomyopathy in Vici syndrome
Egyptian Journal of Medical Human Genetics Q2 2018 10.1016/j.ejmhg.2017.12.003
0 citations 388
18
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]
Egyptian Journal of Medical Human Genetics Q2 2018 10.1016/j.ejmhg.2018.04.004
0 citations 386

Publication Activity

Journals Published In

Egyptian Journal of Medical Human Genetics
🇪🇬 Q2 AMS 99
Egyptian Journal of Medical Human Genetics
🇪🇬 Q2 AMS 98
Egyptian Liver Journal
🇪🇬 Q2 AMS 93