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Rabbani, Bahareh
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1

A comprehensive study of mutation and phenotypic heterogene..:

Hosseinpour, Sareh ; Razmara, Ehsan ; Heidari, Morteza...
Brain and Development.  46 (2024)  4 - p. 167-179 , 2024
Link: https://doi.org/10.1016/..
 
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2

Pancreatitis as a Main Consequence of APOC2-Related Hypertr..:

Rabbani, Bahareh ; Moghadam, Mohadeseh Aghli ; Esmaeili, Shiva...
International Journal of Genomics.  2024 (2024)  - p. 1-13 , 2024
Link: https://doi.org/10.1155/..
 
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3

COLQ-related congenital myasthenic syndrome: An integrative..:

Eshaghian, Tina ; Rabbani, Bahareh ; Badv, Reza Shervin...
neurogenetics.  , 2023
Link: https://doi.org/10.1007/..
 
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4

TCAP gene is not a common cause of cardiomyopathy in Irania..:

Alaei, Zahra ; Zamani, Nasrin ; Rabbani, Bahareh.
European Journal of Medical Research.  28 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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5

P505: Hypertriglyceridemia: Pancreatitis as a common featur..:

Rabbani, Bahareh ; Moghadam, Mohadeseh Aghli ; Esmaeili, Shiva.
Genetics in Medicine Open.  1 (2023)  1 - p. 100552 , 2023
Link: https://doi.org/10.1016/..
 
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6

P506: An integrative view of COLQ-related congenital myasth..:

Eshaghian, Tina ; Rabbani, Bahareh ; Badv, Reza Shervin...
Genetics in Medicine Open.  1 (2023)  1 - p. 100553 , 2023
Link: https://doi.org/10.1016/..
 
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7

Genetics of Cardiovascular Disease and Applications of Gene..:

, In: Practical Cardiology,
Mahdieh, Nejat ; Rabbani, Bahareh ; Maleki, Majid - p. 665-674 , 2022
Link: https://doi.org/10.1016/..
 
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8

Contributors:

, In: Practical Cardiology,
Alemzadeh-Ansari, Mohammad Javad ; Alizadehasl, Azin ; Amin, Ahmad... - p. xix-xxi , 2022
Link: https://doi.org/10.1016/..
 
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9

Corrigendum to "Brown-Vialetto-Van Laere syndrome and Fazio..:

Rabbani, Bahareh ; Bakhshandeh, Mohammad Kazem ; Navaeifar, Mohammad Reza...
Journal of Clinical Neuroscience.  106 (2022)  - p. 244 , 2022
Link: https://doi.org/10.1016/..
 
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10

Genetic testing of leukodystrophies unraveling extensive he..:

Mahdieh, Nejat ; Soveizi, Mahdieh ; Tavasoli, Ali Reza...
Scientific Reports.  11 (2021)  1 - p. , 2021
Link: https://doi.org/10.1038/..
 
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11

Novel cases of pediatric sudden cardiac death secondary to ..:

Rabbani, Bahareh ; Khorgami, Mohammadrafi ; Dalili, Mohammad...
American Journal of Medical Genetics Part A.  185 (2021)  11 - p. 3433-3445 , 2021
Link: https://doi.org/10.1002/..
 
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12

A case of autosomal recessive hypercholesterolemia with a n..:

Nikasa, Parisa ; Rabbani, Bahareh ; Hejazi, Mohammad Saeid...
Clinical Pediatric Endocrinology.  30 (2021)  4 - p. 201-204 , 2021
Link: https://doi.org/10.1297/..
 
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13

Novel disease-causing variants in a cohort of Iranian patie..:

Mahdieh, Nejat ; Sharifi, Ameneh ; Rabbani, Ali...
Clinical Neurology and Neurosurgery.  201 (2021)  - p. 106448 , 2021
Link: https://doi.org/10.1016/..
 
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14

GFAP variants leading to infantile Alexander disease: Pheno..:

Heshmatzad, Katayoun ; Haghi Panah, Mahya ; Tavasoli, Ali Reza...
Clinical Neurology and Neurosurgery.  207 (2021)  - p. 106754 , 2021
Link: https://doi.org/10.1016/..
 
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15

A systematic review of LDLR, PCSK9, and APOB variants in As..:

Mahdieh, Nejat ; Heshmatzad, Katayoun ; Rabbani, Bahareh
Atherosclerosis.  305 (2020)  - p. 50-57 , 2020
Link: https://doi.org/10.1016/..
 
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