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Al-Hassnan, Zuhair
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1

Correction: Expert Group Consensus on early diagnosis and m..:

Al-Hassnan, Zuhair ; Al Hashmi, Nadia ; Makhseed, Nawal...
Orphanet Journal of Rare Diseases.  18 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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2

Expert Group Consensus on early diagnosis and management of..:

Al-Hassnan, Zuhair ; Hashmi, Nadia Al ; Makhseed, Nawal...
Orphanet Journal of Rare Diseases.  17 (2022)  1 - p. , 2022
Link: https://doi.org/10.1186/..
 
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3

Biallelic loss of LDB3 leads to a lethal pediatric dilated ..:

Koopmann, Tamara T. ; Jamshidi, Yalda ; Naghibi-Sistani, Mohammad...
European Journal of Human Genetics.  31 (2022)  1 - p. 97-104 , 2022
Link: https://doi.org/10.1038/..
 
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4

Spectrum of mutations underlying Propionic acidemia and fur..:

Al-Hamed, Mohamed H. ; Imtiaz, Faiqa ; Al-Hassnan, Zuhair...
Molecular Genetics and Metabolism Reports.  18 (2019)  - p. 22-29 , 2019
Link: https://doi.org/10.1016/..
 
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5

Validation of Ion TorrentTM Inherited Disease Panel with th..:

Mustafa, Abeer E. ; Faquih, Tariq ; Baz, Batoul...
Genes.  9 (2018)  5 - p. 267 , 2018
Link: https://doi.org/10.3390/..
 
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6

The effects of low protein products availability on growth ..:

Handoom, Bedour ; Megdad, Eman ; Al-Qasabi, Dana...
International Journal of Pediatrics and Adolescent Medicine.  5 (2018)  2 - p. 60-68 , 2018
Link: https://doi.org/10.1016/..
 
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7

Twenty novel mutations in BCKDHA , BCKDHB and DBT genes in ..:

Imtiaz, Faiqa ; Al-Mostafa, Abeer ; Allam, Rabab...
Molecular Genetics and Metabolism Reports.  11 (2017)  - p. 17-23 , 2017
Link: https://doi.org/10.1016/..
 
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8

Hemophagocytic lymphohistiocytosis: A rare cause of recurre..:

Sulaiman, Raashda Ainuddin ; Shaheen, Marwan Yassin ; Al-Zaidan, Hamad...
Intractable & Rare Diseases Research.  5 (2016)  3 - p. 227-230 , 2016
Link: https://doi.org/10.5582/..
 
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9

Identification of mutations causing hereditary tyrosinemia ..:

Imtiaz, Faiqa ; Rashed, Mohamed S. ; Al-Mubarak, Bashayer...
Molecular Genetics and Metabolism.  104 (2011)  4 - p. 688-690 , 2011
Link: https://doi.org/10.1016/..
 
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10

A novel X-linked disorder with developmental delay and auti..:

Kaya, Namik ; Colak, Dilek ; Albakheet, Albandary...
Annals of Neurology.  71 (2011)  4 - p. 498-508 , 2011
Link: https://doi.org/10.1002/..
 
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11

Novel FBP1 gene mutations in Arab patients with fructose-1,..:

Faiyaz-Ul-Haque, Muhammad ; Al-Owain, Mohammed ; Al-Dayel, Fouad...
European Journal of Pediatrics.  168 (2009)  12 - p. 1467-1471 , 2009
Link: https://doi.org/10.1007/..
 
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12

Preimplantation genetic diagnosis of Morquio disease: PGD F..:

Qubbaj, Wafa ; Al-Aqeel, Aida I. ; Al-Hassnan, Zuhair...
Prenatal Diagnosis.  28 (2008)  10 - p. 900-903 , 2008
Link: https://doi.org/10.1002/..
 
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13

Identification of Gaucher disease mutations found in Saudi ..:

Kaya, Namik ; Al-Zahrani, Fatima ; Al-Odaib, Ali...
Blood Cells, Molecules, and Diseases.  41 (2008)  2 - p. 200-201 , 2008
Link: https://doi.org/10.1016/..
 
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14

Rapid UPLC-MS/MS method for routine analysis of plasma pris..:

Al-Dirbashi, Osama Y. ; Santa, Tomofumi ; Rashed, Mohamed S....
Journal of Lipid Research.  49 (2008)  8 - p. 1855-1862 , 2008
Link: https://doi.org/10.1194/..
 
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15

Genome-wide gene expression profiling and mutation analysis..:

Kaya, Namik ; Imtiaz, Faiqa ; Colak, Dilek...
Genetics in Medicine.  10 (2008)  9 - p. 675-684 , 2008
Link: https://doi.org/10.1097/..
 
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