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Alkuraya, Hisham S
497  Ergebnisse:
Personensuche X
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1

Acute endophthalmitis caused by Staphylococcus lugdunesis a..:

Alkuraya, Hisham S. ; Al-kharashi, Abdullah S. ; Alharthi, Essam.
International Ophthalmology.  29 (2008)  5 - p. 411-413 , 2008
Link: https://doi.org/10.1007/..
 
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2

Ocular manifestations in Kabuki syndrome: the first report ..:

Chaudhry, Imtiaz A. ; Shamsi, Farrukh A. ; Alkuraya, Hisham S..
International Ophthalmology.  28 (2007)  2 - p. 131-134 , 2007
Link: https://doi.org/10.1007/..
 
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3

Argon Laser Photoablation for Treating Benign Pigmented Con..:

Alsharif, Abdulrahman M ; Al-Gehedan, Saeed M ; Alasbali, Tariq...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4968145/.  , 2016
Link: http://www.ncbi.nlm.nih...
 
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4

Lack of Correlation Between Diabetic Macular Edema and Thic..:

Alkuraya, Hisham S ; Al-Gehedan, Saeed M ; Alsharif, Abdulrahman M...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4968144/.  , 2016
Link: http://www.ncbi.nlm.nih...
 
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5

Recessive Mutations in ELOVL4 Cause Ichthyosis, Intellectua..:

Aldahmesh, Mohammed A ; Mohamed, Jawahir Y ; Alkuraya, Hisham S...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3234380.  , 2011
Link: http://www.ncbi.nlm.nih...
 
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6

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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7

Front Cover:

Alkuraya, Hisham ; Patel, Nisha ; Ibrahim, Niema...
Clinical Genetics.  97 (2020)  3 - p. , 2020
Link: https://doi.org/10.1111/..
 
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8

Further delineation of HIDEA syndrome:

Maddirevula, Sateesh ; Ben‐Omran, Tawfeg ; AlMureikhi, Mariam...
American Journal of Medical Genetics Part A.  182 (2020)  12 - p. 2999-3006 , 2020
Link: https://doi.org/10.1002/..
 
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9

Phenotypic delineation of the retinal arterial macroaneurys..:

Alkuraya, Hisham ; Patel, Nisha ; Ibrahim, Niema...
Clinical Genetics.  97 (2019)  3 - p. 447-456 , 2019
Link: https://doi.org/10.1111/..
 
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10

Correction: Corrigendum: Autozygosity reveals recessive mut..:

Monies, Dorota ; Maddirevula, Sateesh ; Kurdi, Wesam...
Genetics in Medicine.  20 (2018)  3 - p. 380 , 2018
Link: https://doi.org/10.1038/..
 
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11

Congenital glaucoma and CYP1B1: an old story revisited:

Alsaif, Hessa S. ; Khan, Arif O. ; Patel, Nisha...
Human Genetics.  138 (2018)  8-9 - p. 1043-1049 , 2018
Link: https://doi.org/10.1007/..
 
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12

Autozygosity reveals recessive mutations and novel mechanis..:

Monies, Dorota ; Maddirevula, Sateesh ; Kurdi, Wesam...
Genetics in Medicine.  19 (2017)  10 - p. 1144-1150 , 2017
Link: https://doi.org/10.1038/..
 
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13

Treatment of retinitis pigmentosa due to MERTK mutations by..:

Ghazi, Nicola G. ; Abboud, Emad B. ; Nowilaty, Sawsan R....
Human Genetics.  135 (2016)  3 - p. 327-343 , 2016
Link: https://doi.org/10.1007/..
 
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14

Expanding the clinical, allelic, and locus heterogeneity of..:

Patel, Nisha ; Aldahmesh, Mohammed A. ; Alkuraya, Hisham...
Genetics in Medicine.  18 (2016)  6 - p. 554-562 , 2016
Link: https://doi.org/10.1038/..
 
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15

Exome-based case–control association study using extreme ph..:

Shtir, Corina ; Aldahmesh, Mohammed A. ; Al-Dahmash, Saad...
Human Genetics.  135 (2015)  2 - p. 193-200 , 2015
Link: https://doi.org/10.1007/..
 
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