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Search Results - Rasoulinezhad, Maryam
Search Results - Rasoulinezhad, Maryam
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Primary and Secondary Microcephaly, Global Developmental Delay, and Seizure in Two Siblings Caused by a Novel Missense Variant in the ZNF335 Gene
by
Tavasoli, Ali Reza
,
Memar, Elmira Haji Esmaeil
,
Ashrafi, Mahmoud Reza
,
Hosseini, Seyed Mohammad Mahdi
,
Haghighi, Roya
,
Ghabeli, Homa
,
Pourbakhtyaran, Elham
,
Rasoulinezhad, Maryam
,
Mohammadi, Pouria
,
Heidari, Morteza
Published in
Journal of molecular neuroscience
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Symptomatic care of late-onset Alexander disease presenting with area postrema-like syndrome with prednisolone; a case report
by
Zardadi, Safoura
,
Razmara, Ehsan
,
Rasoulinezhad, Maryam
,
Babaei, Meisam
,
Ashrafi, Mohammad Reza
,
Pak, Neda
,
Garshasbi, Masoud
,
Tavasoli, Ali Reza
Published in
BMC pediatrics
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CEP104 gene may involve in the pathogenesis of a new developmental disorder other than joubert syndrome
by
Badv, Reza Shervin
,
Mahdiannasser, Mojdeh
,
Rasoulinezhad, Maryam
,
Habibi, Laleh
,
Rashidi-Nezhad, Ali
Published in
Molecular biology reports
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Leukoencephalopathy in Al‐Raqad syndrome: Expanding the clinical and neuroimaging features caused by a biallelic novel missense variant in DCPS
by
Masoudi, Maryam
,
Bereshneh, Ali Hosseini
,
Rasoulinezhad, Maryam
,
Ashrafi, Mahmoud Reza
,
Garshasbi, Masoud
,
Tavasoli, Ali Reza
Published in
American journal of medical genetics. Part A
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Defective complex III mitochondrial respiratory chain due to a novel variant in CYC1 gene masquerades acute demyelinating syndrome or Leber hereditary optic neuropathy
by
Heidari, Erfan
,
Rasoulinezhad, Maryam
,
Pak, Neda
,
Reza Ashrafi, Mahmoud
,
Heidari, Morteza
,
Banwell, Brenda
,
Garshasbi, Masoud
,
Reza Tavasoli, Ali
Published in
Mitochondrion
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Expanding the clinical and neuroimaging features of NKX6-2-related hereditary spastic ataxia type 8
by
Hosseini Bereshneh, Ali
,
Hosseipour, Sareh
,
Rasoulinezhad, Maryam Sadat
,
Pak, Neda
,
Garshasbi, Masoud
,
Tavasoli, Ali Reza
Published in
European journal of medical genetics
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Leukoencephalopathy in Al-Raqad syndrome: Expanding the clinical and neuroimaging features caused by a biallelic novel missense variant in DCPS
by
Masoudi, Maryam
,
Bereshneh, Ali Hosseini
,
Rasoulinezhad, Maryam
,
Ashrafi, Mahmoud Reza
,
Garshasbi, Masoud
,
Tavasoli, Ali Reza
Published in
American journal of medical genetics. Part A
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