Miraç Yıldırım (Mirac Yildirim)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 12

Top Topics

Acute Respiratory Distress Syndrome

Mechanical Ventilation

Muscular Dystrophy

Top Venues

Neuropediatrics

Pediatric pulmonology

Acta neurologica Belgica

Clinical neuropharmacology

This page only lists publications with an associated author ORCID identifier.

Publications

Miraç Yıldırım, Gülçin Bilicen Yarenci, Mustafa Berk Genç, Çiğdem İlter Uçar, Secahattin Bayav, Merve Nur Tekin, Ömer Bektaş, Serap Tıraş Teber
VAMP1-Related Congenital Myasthenic Syndrome: A Case Report and Literature Review. Neuropediatrics 55 (3) (2024)
Miraç Yıldırım, Gülçin Bilicen Yarenci, Mustafa Berk Genç, Çiğdem İlter Uçar, Secahattin Bayav, Merve Nur Tekin, Ömer Bektaş, Serap Tıraş Teber
VAMP1-Related Congenital Myasthenic Syndrome: A Case Report and Literature Review. Neuropediatrics 55 (3) (2024)
Miraç Yıldırım, Gülçin Bilicen Yarenci, Mustafa Berk Genç, Çiğdem İlter Uçar, Secahattin Bayav, Merve Nur Tekin, Ömer Bektaş, Serap Tıraş Teber
VAMP1-Related Congenital Myasthenic Syndrome: A Case Report and Literature Review. Neuropediatrics (2024)
Miraç Yıldırım, Gülçin Bilicen Yarenci, Mustafa Berk Genç, Çiğdem İlter Uçar, Secahattin Bayav, Merve Nur Tekin, Ömer Bektaş, Serap Tıraş Teber
VAMP1-Related Congenital Myasthenic Syndrome: A Case Report and Literature Review. Neuropediatrics 55 (3) (2024)
Yavuz Sayar, Miraç Yıldırım, Serap Tıraş Teber
Management of neurological problems in children on home invasive mechanical ventilation. Pediatric pulmonology (2023)
Yavuz Sayar, Miraç Yıldırım, Serap Tıraş Teber
Management of neurological problems in children on home invasive mechanical ventilation. Pediatric pulmonology 59 (8) (2023)
Nurşah Yeniay Süt, Miraç Yıldırım, Ömer Bektaş, Tanıl Kendirli, Serap Tıraş Teber
A Case of Multidrug-Resistant Lance-Adams Syndrome Successfully Treated With Phenobarbital. Clinical neuropharmacology (2022)
Nurşah Yeniay Süt, Miraç Yıldırım, Ömer Bektaş, Mert Altıntaş, Serap Teber
The diagnostic challenges of congenital mirror movements and hand stereotypies in a case with TUBB3-associated tubulinopathy. Acta neurologica Belgica 122 (1) (2022)
Çiğdem İlter Uçar, Miraç Yıldırım, Yavuz Sayar, Süleyman Şahin, Serap Tıraş Teber
Hypomelanosis of Ito presenting with unilateral dilation of Virchow-Robin spaces: a case report. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 37 (9) (2021)
Miraç Yıldırım, Hatice Koçak Eker, Melih Timuçin Doğan
A homozygous mutation in the POMT2 gene in four siblings with limb-girdle muscular dystrophy 2N. Turkish archives of pediatrics 56 (1) (2021)
Miraç Yıldırım, Avni Merter Keceli, Nazmi Simsek, Celebi Kocaoglu
Fulminant acute hemorrhagic leukoencephalopathy: ineffective treatment with immunotherapy. Acta neurologica Belgica (2021)
Miraç Yıldırım, Rahsan Gocmen, Bahadir Konuskan, Şafak Parlak Sağol, Dilek Yalnizoglu, Banu Anlar
Acute Cerebellitis or Postinfectious Cerebellar Ataxia? Clinical and Imaging Features in Acute Cerebellitis. Journal of child neurology 35 (6) (2020)