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Alsagheir, Afaf
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1

Information needs on type 1 diabetes mellitus (T1DM) and it..:

Muhammed Elamin, Sasha ; Muhamad Arshad, Nur Fitrah ; Md Redzuan, Adyani...
BMJ Open.  14 (2024)  4 - p. e079606 , 2024
Link: https://doi.org/10.1136/..
 
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2

Modern approaches to the management of homozygous familial ..:

Al-Ashwal, Abdullah ; Alsagheir, Afaf ; Al Dubayee, Mohammed...
Journal of Clinical Lipidology.  18 (2024)  2 - p. e132-e141 , 2024
Link: https://doi.org/10.1016/..
 
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3

Analysis of disease characteristics of a large patient coho..:

Al Yaarubi, Saif ; Alsagheir, Afaf ; Al Shidhani, Azza...
Orphanet Journal of Rare Diseases.  19 (2024)  1 - p. , 2024
Link: https://doi.org/10.1186/..
 
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4

Clinical characteristics and long-term management for patie..:

Alsagheir, Afaf ; Al-Ashwal, Abdullah ; Binladen, Amal...
Frontiers in Endocrinology.  15 (2024)  - p. , 2024
Link: https://doi.org/10.3389/..
 
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5

Hajdu-Cheney syndrome with a novel variant in NOTCH2 gene: ..:

Abdelkarim, Mariam ; Alageel, Dalal ; Ahsan, Faridul...
Bone Reports.  19 (2023)  - p. 101709 , 2023
Link: https://doi.org/10.1016/..
 
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6

Management of childhood-onset growth hormone deficiency in ..:

AlMutair, Angham ; Alsagheir, Afaf ; AlShammary, Afaf...
International Journal of Pediatrics and Adolescent Medicine.  10 (2023)  2 - p. 21-30 , 2023
Link: https://doi.org/10.4103/..
 
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7

The clinical characteristics and quality of life of 248 ped..:

Shafaay, Edi A. ; Aldriweesh, Mohammed A. ; Aljahdali, Ghadeer L....
Frontiers in Endocrinology.  14 (2023)  - p. , 2023
Link: https://doi.org/10.3389/..
 
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8

Munchausen syndrome by proxy: a case report:

Alkhattabi, Fadiah ; Bamogaddam, Israa ; Alsagheir, Afaf..
Journal of Medical Case Reports.  17 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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9

The morbid genome of ciliopathies: an update:

Shamseldin, Hanan E. ; Shaheen, Ranad ; Ewida, Nour...
Genetics in Medicine.  24 (2022)  4 - p. 966 , 2022
Link: https://doi.org/10.1016/..
 
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10

A Rare Case of Adenosine Deaminase tRNA-Specific 3 Mutation..:

AlDhalaan, Waheeb ; Syed, Faaezuddin ; Javaid, Haroon A..
Cureus.  , 2021
Link: https://doi.org/10.7759/..
 
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11

A Unique Genotype of Pseudohypoaldosteronism Type 1b in a H..:

Alzahrani, Ali S ; Alswailem, Meshael ; Abbas, Bassam Bin...
Journal of the Endocrine Society.  5 (2021)  8 - p. , 2021
Link: https://doi.org/10.1210/..
 
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12

Molecular genetics of disorders of sex development in a hig..:

Alswailem, Meshael ; Alsagheir, Afaf ; Abbas, Bassam Ben..
The Journal of Steroid Biochemistry and Molecular Biology.  208 (2021)  - p. 105736 , 2021
Link: https://doi.org/10.1016/..
 
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13

Analysis of transcript-deleterious variants in Mendelian di..:

Maddirevula, Sateesh ; Kuwahara, Hiroyuki ; Ewida, Nour...
Genome Biology.  21 (2020)  1 - p. , 2020
Link: https://doi.org/10.1186/..
 
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14

The morbid genome of ciliopathies: an update:

Shamseldin, Hanan E. ; Shaheen, Ranad ; Ewida, Nour...
Genetics in Medicine.  22 (2020)  6 - p. 1051-1060 , 2020
Link: https://doi.org/10.1038/..
 
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15

Expanding the phenome and variome of skeletal dysplasia:

Maddirevula, Sateesh ; Alsahli, Saud ; Alhabeeb, Lamees...
Genetics in Medicine.  20 (2018)  12 - p. 1609-1616 , 2018
Link: https://doi.org/10.1038/..
 
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