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El-Khashab, Heba Y.
20  results:
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1

A possible association between elevated serum levels of bra..:

Mostafa, Gehan A. ; El-Khashab, Heba Y. ; AL-Ayadhi, Laila Y.
Journal of Neuroimmunology.  280 (2015)  - p. 16-20 , 2015
Link: https://doi.org/10.1016/..
 
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2

A Survey to Identify the Current Management of Cow's Milk D..:

Bahbah, Wael A. ; ElHodhod, Mostafa ; Salah, Mohamed...
Nutrients.  14 (2022)  5 - p. 1067 , 2022
Link: https://doi.org/10.3390/..
 
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3

Hereditary Hyperekplexia in Saudi Arabia:

Aldhilan, Amal ; Alhakeem, Afnan ; Al Hajjaj, Sumayah...
Pediatric Neurology.  134 (2022)  - p. 78-82 , 2022
Link: https://doi.org/10.1016/..
 
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4

A Survey to Identify the Current Management of Cow's Milk D..:

Wael A. Bahbah ; Mostafa ElHodhod ; Mohamed Salah...
https://www.mdpi.com/2072-6643/14/5/1067.  , 2022
Link: https://doi.org/10.3390/..
 
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5

A Survey to Identify the Current Management of Cow's Milk D..:

Wael A. Bahbah ; Mostafa ElHodhod ; Mohamed Salah...
Nutritional Immunology.  , 2022
Link: https://doi.org/10.3390/..
 
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6

A Survey to Identify the Current Management of Cow's Milk D..:

Bahbah, Wael A ; ElHodhod, Mostafa ; Salah, Mohamed...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8912394/.  , 2022
Link: http://www.ncbi.nlm.nih...
 
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7

Esophageal Motility in patients with type-1 diabetes mellit..:

Salem, Mona ; Monir, Eman ; El Din, HeshamEzz.
Diabetes Research and Clinical Practice.  50 (2000)  - p. 56-57 , 2000
Link: https://doi.org/10.1016/..
 
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8

Autozygome and high throughput confirmation of disease gene..:

Maddirevula, Sateesh ; Alzahrani, Fatema ; Al-Owain, Mohammed...
Genetics in Medicine.  21 (2019)  3 - p. 736-742 , 2019
Link: https://doi.org/10.1038/..
 
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9

The many faces of peroxisomal disorders: Lessons from a lar..:

Alshenaifi, Jumanah ; Ewida, Nour ; Anazi, Shams...
Clinical Genetics.  95 (2018)  2 - p. 310-319 , 2018
Link: https://doi.org/10.1111/..
 
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10

The landscape of genetic diseases in Saudi Arabia based on ..:

Monies, Dorota ; Abouelhoda, Mohamed ; AlSayed, Moeenaldeen...
Human Genetics.  136 (2017)  8 - p. 921-939 , 2017
Link: https://doi.org/10.1007/..
 
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11

Novel copy number variants and major limb reduction malform..:

Shamseldin, Hanan E. ; Anazi, Shams ; Wakil, Salma M....
American Journal of Medical Genetics Part A.  170 (2016)  5 - p. 1245-1250 , 2016
Link: https://doi.org/10.1002/..
 
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12

Pathogenic variants inKCTD7perturb neuronal K+fluxes and gl..:

Moen, Marivi Nabong ; Fjær, Roar ; Hamdani, El Hassan...
Brain.  139 (2016)  12 - p. 3109-3120 , 2016
Link: https://doi.org/10.1093/..
 
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13

The clinical utility of molecular karyotyping for neurocogn..:

Al-Qattan, Sarah M. ; Wakil, Salma M. ; Anazi, Shamsa...
Genetics in Medicine.  17 (2015)  9 - p. 719-725 , 2015
Link: https://doi.org/10.1038/..
 
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14

Mutation in GM2A Leads to a ProgressiveChorea-dementia Synd..:

Salih, Mustafa A. ; Seidahmed, Mohammed Z. ; El Khashab, Heba Y....
Tremor and Other Hyperkinetic Movements.  5 (2015)  0 - p. 306 , 2015
Link: https://doi.org/10.5334/..
 
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15

A newly recognized autosomal recessive syndrome affecting n..:

Salih, Mustafa A. ; Tzschach, Andreas ; Oystreck, Darren T....
American Journal of Medical Genetics Part A.  161 (2013)  6 - p. 1207-1213 , 2013
Link: https://doi.org/10.1002/..
 
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