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Hamza, Nishath
22  Ergebnisse:
Personensuche X
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1

First Report of a Derivative Chromosome 13 with a Duplicate..:

Hamza, Nishath ; Al-Araimi, Musallam ; Al Salmani, Kamla.
Sultan Qaboos University Medical Journal [SQUMJ].  , 2022
Link: https://doi.org/10.18295..
 
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2

A Novel SPINK5 Gene Mutation Associated with Netherton Synd..:

Hamza, Nishath ; Al Sukaiti, Nashat ; Ahmed, Khwater AM...
Sultan Qaboos University Medical Journal [SQUMJ].  21 (2021)  4 - p. 652-656 , 2021
Link: https://doi.org/10.18295..
 
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3

A first case report of hypohidrotic ectodermal dysplasia fr..:

Al‐Araimi, Musallam ; Hamza, Nishath ; Al Hosni, Aliya.
Clinical Case Reports.  8 (2020)  4 - p. 716-718 , 2020
Link: https://doi.org/10.1002/..
 
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4

Rare NF1 microdeletion syndrome in an Omani patient:

Al‐Araimi, Musallam ; Hamza, Nishath ; Al Yahmadi, Ali...
Clinical Case Reports.  6 (2018)  12 - p. 2424-2426 , 2018
Link: https://doi.org/10.1002/..
 
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5

Repository of mutations from Oman: The entry point to a nat..:

Rajab, Anna ; Hamza, Nishath ; Al Harasi, Salma...
F1000Research.  4 (2015)  - p. 891 , 2015
Link: https://doi.org/10.12688..
 
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6

B-cell populations and sub-populations in Sjögren's syndrom:

Hamza, Nishath ; Bos, Nicolaas A. ; Kallenberg, Cees G.M.
La Presse Médicale.  41 (2012)  9 - p. e475-e483 , 2012
Link: https://doi.org/10.1016/..
 
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7

First Report of a Derivative Chromosome 13 with a Duplicate..:

Hamza, Nishath ; Al-Araimi, Musallam ; Al Salmani, Kamla.
https://journals.squ.edu.om/index.php/squmj/article/view/5035/3457.  , 2023
Link: https://journals.squ.edu..
 
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8

First Report of a Derivative Chromosome 13 with a Duplicate..:

Hamza, Nishath ; Al-Araimi, Musallam ; Al Salmani, Kamla.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10292596/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
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9

A Novel SPINK5 Gene Mutation Associated with Netherton Synd..:

Hamza, Nishath ; Al Sukaiti, Nashat ; Ahmed, Khwater AM...
https://journals.squ.edu.om/index.php/squmj/article/view/4227/3113.  , 2021
Link: https://journals.squ.edu..
 
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10

Hereditary Paraganglioma in an Omani Family:

Pambinezhthu, Fathima ; Hamza, Nishath ; Al Kharusi, Manal...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7897353/.  , 2021
Link: http://www.ncbi.nlm.nih...
 
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11

A Novel SPINK5 Gene Mutation Associated with Netherton Synd..:

Hamza, Nishath ; Al Sukaiti, Nashat ; Ahmed, Khwater A.M...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8631226/.  , 2021
Link: http://www.ncbi.nlm.nih...
 
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12

A first case report of hypohidrotic ectodermal dysplasia fr..:

Al‐Araimi, Musallam ; Hamza, Nishath ; Al Hosni, Aliya.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7141724/.  , 2020
Link: http://www.ncbi.nlm.nih...
 
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13

Rare NF1 microdeletion syndrome in an Omani patient:

Al‐Araimi, Musallam ; Hamza, Nishath ; Al Yahmadi, Ali...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6293151/.  , 2018
Link: http://www.ncbi.nlm.nih...
 
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14

Acquiring new N-glycosylation sites in variable regions of ..:

Visser, Annie ; Hamza, Nishath ; Kroese, Frans G M.
https://research.rug.nl/en/publications/eeba8db5-26fe-45ff-b8c3-60297ef72bf0.  , 2018
Link: https://hdl.handle.net/1..
 
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15

Genetic Mutations Associated with Neonatal Diabetes Mellitu..:

Al Senani, Aisha ; Hamza, Nishath ; AlAzkawi, Hanan...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6853791/.  , 2018
Link: http://www.ncbi.nlm.nih...
 
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