Suchergebnisse - "Haliloglu, Goknur"

PubPharm (162)

71

Acute Abducens Nerve Paralysis in the Pediatric Emergency Department : Analysis of 14 Patients

enthalten in: Pediatric emergency care | 2016

von Teksam, O. | Gultekingil, A. | Konuskan, B. | +3

ErratumIn: Pediatr Emerg Care. 2021 Mar 1;37(3):190. - PMID 33651764

72

Susceptibility-Weighted Magnetic Resonance Imaging Findings of Two Pediatric Migraine Patients with Aura

enthalten in: Neuropediatrics | 2016

von Gocmen, R. | Gunbey, C. | Arsava, E. | +2

CommentIn: Neuropediatrics. 2016 Jan;47(1):3-4. - PMID 26727294

73

Acute Abducens Nerve Paralysis in the Pediatric Emergency Department: Analysis of 14 Patients

enthalten in: Pediatric emergency care | 2016

von Teksam, O. | Keser, A. | Konuskan, B. | +3

74

Hereditary Dopamine Transporter Deficiency Syndrome: Challenges in Diagnosis and Treatment

enthalten in: Neuropediatrics | 2016

von Yildiz, Y. | Pektas, E. | Tokatli, A. | +1

75

Challenges in pediatric chronic inflammatory demyelinating polyneuropathy

enthalten in: Neuromuscular disorders | 2016

von Haliloğlu, G. | Yüksel, D. | Temoçin, C. | +1

76

Challenges in pediatric chronic inflammatory demyelinating polyneuropathy

enthalten in: Neuromuscular disorders | 2016

von Haliloğlu, G. | Yüksel, D. | Temuçin, C. | +1

77

Clinical characteristics of megaconial congenital muscular dystrophy due to choline kinase beta gene defects in a series of 15 patients

enthalten in: Journal of inherited metabolic disease | 2015

von Haliloglu, G. | Talim, B. | Sel, C. | +1

78

Next generation sequencing in a large cohort of patients presenting with neuromuscular disease before or at birth

enthalten in: Orphanet journal of rare diseases | 2015

von Todd, E. | Yau, K. | Ong, R. | +23

79

Next generation sequencing in a large cohort of patients presenting with neuromuscular disease before or at birth

enthalten in: Orphanet journal of rare diseases | 2015

von Todd, E. | Yau, K. | Ong, R. | +23

80

Evidence-based guideline summary : Evaluation, diagnosis, and management of congenital muscular dystrophy: Report of the Guideline Development Subcommittee of the American Academy of Neurology and the Practice Issues Review Panel of the American Association of Neuromuscular & Electrodiagnostic Medicine

enthalten in: Neurology | 2015

von Haliloglu, G. | Topaloglu, H.

CommentOn: Neurology. 2015 Mar 31;84(13):1369-78. - PMID 25825463