Ahmet Sami Guven
Overview
Explore the profile of Ahmet Sami Guven including associated specialties, affiliations and a list of published articles.
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Articles
34
Citations
119
Followers
0
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Recent Articles
1.
Bilgec N, Caliskan B, Eravci S, Guven A, Caksen H
Clin Dysmorphol
. 2025 Jan;
PMID: 39807608
Introduction: Spondyloepimetaphyseal dysplasia with joint laxity type 1 (SEMD-JL1) is an extremely rare skeletal dysplasia belonging to a group of disorders called linkeropathies. It is characterized by skeletal and connective...
2.
Caksen H, Yilmaz S, Guven A, Guldibi F, Erdi M, Acikgozoglu S
Neurol Neurochir Pol
. 2023 Jan;
57(4):397-400.
PMID: 36661106
No abstract available.
3.
Caksen H, Yilmaz S, Guven A, Guldibi F, Acikgozoglu S
Childs Nerv Syst
. 2022 Nov;
39(1):21-24.
PMID: 36357722
No abstract available.
4.
Cetin F, Baris Usta M, Aydin S, Guven A
Clin EEG Neurosci
. 2021 Dec;
53(5):406-417.
PMID: 34923863
Complexity analysis is a method employed to understand the activity of the brain. The effect of methylphenidate (MPH) treatment on neuro-cortical complexity changes is still unknown. This study aimed to...
5.
Caksen H, Koseoglu F, Guven A, Altunhan H, Iyisoy M, Acikgozoglu S
Ann Indian Acad Neurol
. 2021 Jul;
24(2):227-233.
PMID: 34220067
Background: Perinatal stroke encompasses a heterogeneous group of focal neurological injuries early in brain development. In this study, we aimed to compare risk and prognostic factors in preterm and term...
6.
Koc G, Bayram N, Guven A, Inan D, Kaya A
Noro Psikiyatr Ars
. 2020 Sep;
57(3):257-260.
PMID: 32952431
Neuromyelitis Optica spectrum disorder (NMO-SD) is a rare demyelinating disease detected in pediatric patients affecting the primary optic nerve and spinal cord. Clinical findings might overlap with other demyelinating diseases...
7.
Caksen H, Koseoglu F, Guven A, Altunhan H, Acikgozoglu S
Childs Nerv Syst
. 2020 Jul;
36(12):2905-2907.
PMID: 32725467
No abstract available.
8.
Wang H, Bayram A, Sprute R, Ozdemir O, Cooper E, Pergande M, et al.
Front Neurosci
. 2019 Nov;
13:974.
PMID: 31680794
Charcot-Marie-Tooth type 4 (CMT4) is an autosomal recessive severe form of neuropathy with genetic heterogeneity. CMT4B1 is caused by mutations in the myotubularin-related 2 ( gene and as a member...
9.
Celik S, Baratali E, Guven A, Torun Y
Seizure
. 2018 Sep;
61:153-157.
PMID: 30170299
Purpose: Although there is a higher risk of structural cardiac disease in people with epilepsy, there is no detailed advanced analysis of cardiac functions in patients with epilepsy. This study...
10.
Ergul A, Altug U, Aydin K, Guven A, Torun Y
Neuroradiol J
. 2017 Jan;
30(2):164-167.
PMID: 28059631
Acute necrotizing encephalopathy is characterized by multiple, symmetrical lesions involving the thalamus, brainstem, cerebellum, and white matter and develops secondarily to viral infections. Influenza viruses are the most common etiological...