Demirkıran, Meltem
72  Ergebnisse:
Personensuche X
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5

MYO1H is a novel candidate gene for autosomal dominant pure..:

Selçuk, Ece ; Kırımtay, Koray ; Temizci, Benan...
Molecular Genetics and Genomics.  297 (2022)  4 - p. 1141-1150 , 2022
 
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6

The Turkish experience of COVID-19 infection in people with..:

Sen, Sedat ; Tuncer, Asli ; Ozakbas, Serkan...
Multiple Sclerosis and Related Disorders.  58 (2022)  - p. 103399 , 2022
 
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8

Is RLS a harbinger and consequence of MS?: Striking results..:

Sevim, Serhan ; Demirkıran, Meltem ; Terzi, Murat...
Multiple Sclerosis and Related Disorders.  42 (2020)  - p. 102055 , 2020
 
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10

Comparative analysis of fingolimod versus teriflunomide in ..:

Boz, Cavit ; Terzi, Murat ; Özer, Bilge...
Multiple Sclerosis and Related Disorders.  36 (2019)  - p. 101376 , 2019
 
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13

A Rare Cause of Myelopathy: Os Odontoideum:

Balal, Mehmet ; Şanlı, Zeynep Selcan ; Demirkıran, Meltem
Turkish Journal Of Neurology.  24 (2018)  2 - p. 184-185 , 2018
 
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14

Cystic Lesions in Spinal Astrocytoma:

Evlice, Ahmet ; İşcan, Dilek ; Demirkıran, Meltem
Turkish Journal Of Neurology.  22 (2016)  2 - p. 90-91 , 2016
 
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