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Al Hashmi, Nadia
82
results:
Search for persons
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Online (82)
Mediatypes
Articles (Online) (35)
Bookchapter (Online) (6)
OpenAccess-fulltext (41)
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1
A founder mutation in CA5A causing intrafamilial and interf..:
Al‐Thihli, Khalid
;
Al Hashmi, Nadia
;
Al Balushi, Aaisha
...
JIMD Reports. 65 (2024) 4 - p. 226-232 , 2024
Link:
https://doi.org/10.1002/..
?
2
Genetic analysis and outcomes of Omani children with steroi..:
Al Riyami, Mohamed S.
;
Al Alawi, Intisar
;
Al Gaithi, Badria
...
Molecular Genetics & Genomic Medicine. 11 (2023) 9 - p. , 2023
Link:
https://doi.org/10.1002/..
?
3
Domino liver transplantation for maple syrup urine disease ..:
Kumar, Vikram
;
Gautam, Vipul
;
Agarwal, Shaleen
...
Pediatric Transplantation. 27 (2023) 8 - p. , 2023
Link:
https://doi.org/10.1111/..
?
4
Expanding the clinical spectrum of cytosolic phosphoenolpyr..:
Al Busaidi, Marwa
;
Mohamed, Feda E.
;
Al-Ajmi, Eiman
...
Orphanet Journal of Rare Diseases. 18 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1186/..
?
5
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/..
?
6
Uptake of prenatal genetic diagnosis and termination of pre..:
Bruwer, Zandré
;
Al Ubaidani, Salwa
;
Al Kharusi, Khalsa
...
Journal of Community Genetics. 13 (2022) 3 - p. 303-311 , 2022
Link:
https://doi.org/10.1007/..
?
7
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/..
?
8
Loss of DIAPH1 causes SCBMS, combined immunodeficiency, and..:
Kaustio, Meri
;
Nayebzadeh, Naemeh
;
Hinttala, Reetta
...
Journal of Allergy and Clinical Immunology. 148 (2021) 2 - p. 599-611 , 2021
Link:
https://doi.org/10.1016/..
?
9
Combining exome/genome sequencing with data repository anal..:
Bertoli-Avella, Aida M.
;
Kandaswamy, Krishna K.
;
Khan, Suliman
...
Genetics in Medicine. 23 (2021) 8 - p. 1551-1568 , 2021
Link:
https://doi.org/10.1038/..
?
10
Primary Hyperoxaluria Type 1 in 18 Children: Genotyping and..:
Al Riyami, Mohamed S.
;
Al Ghaithi, Badria
;
Al Hashmi, Nadia
.
International Journal of Nephrology. 2015 (2015) - p. 1-6 , 2015
Link:
https://doi.org/10.1155/..
?
11
Book Reviews:
Hashmi, Nadia
European Journal of Cultural Studies. 6 (2003) 2 - p. 253-255 , 2003
Link:
https://doi.org/10.1177/..
?
12
Expanding the clinical spectrum of cytosolic phosphoenolpyr..:
Al Busaidi, Marwa
;
Mohamed, Feda E
;
Al-Ajmi, Eiman
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10625263/. , 2023
Link:
http://www.ncbi.nlm.nih...
?
13
Genetic analysis and outcomes of Omani children with steroi..:
Al Riyami, Mohamed S
;
Al Alawi, Intisar
;
Al Gaithi, Badria
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10496054/. , 2023
Link:
http://www.ncbi.nlm.nih...
?
14
Loss of DIAPH1 causes SCBMS, combined immunodeficiency, and..:
Kaustio, Meri
;
Nayebzadeh, Naemeh
;
Hinttala, Reetta
...
NFR/187615. , 2022
Link:
http://hdl.handle.net/10..
?
15
Loss of DIAPH1 causes SCBMS, combined immunodeficiency, and..:
Kaustio, Meri
;
Nayebzadeh, Naemeh
;
Hinttala, Reetta
...
10.1016/j.jaci.2020.12.656. , 2021
Link:
http://hdl.handle.net/10..
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