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Haliloglu, Goknur
127  results:
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1

European Joint Programme on Rare Diseases workshop: LAMA2-m..:

Smeets, Hubert ; Verbrugge, Bram ; Bulbena, Xavier...
Neuromuscular Disorders.  36 (2024)  - p. 16-22 , 2024
Link: https://doi.org/10.1016/..
 
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2

Validity and reliability of the MetabQoL 1.0 and assessment..:

Ersak, Ayşe Şenol ; Çak, Halime Tuna ; Yıldız, Yılmaz...
Molecular Genetics and Metabolism.  141 (2024)  1 - p. 108117 , 2024
Link: https://doi.org/10.1016/..
 
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3

Electro-clinical features and long-term outcomes in guanidi..:

Yıldız, Yılmaz ; Ardıçlı, Didem ; Göçmen, Rahşan...
European Journal of Paediatric Neurology.  49 (2024)  - p. 66-72 , 2024
Link: https://doi.org/10.1016/..
 
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4

Horizontal gaze palsy with progressive scoliosis: Further e..:

Günbey, Ceren ; Çavdarlı, Büşranur ; Göçmen, Rahşan...
Annals of Clinical and Translational Neurology.  , 2024
Link: https://doi.org/10.1002/..
 
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5

Further expanding the phenotype of anti-Ku antibody associa..:

Batu, Ezgi Deniz ; Şener, Seher ; Haliloğlu, Göknur...
Neuromuscular Disorders.  40 (2024)  - p. 7-15 , 2024
Link: https://doi.org/10.1016/..
 
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6

Proteomic Investigation of Differential Interactomes of Gly..:

Cengiz Winter, Nur ; Karakaya, Mert ; Mosen, Peter...
Journal of Proteome Research.  22 (2023)  9 - p. 3081-3095 , 2023
Link: https://doi.org/10.1021/..
 
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7

Early-onset juvenile dermatomyositis: A tertiary referral c..:

Sener, Seher ; Basaran, Ozge ; Batu, Ezgi Deniz...
Seminars in Arthritis and Rheumatism.  58 (2023)  - p. 152133 , 2023
Link: https://doi.org/10.1016/..
 
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8

Two tales of LPIN1 deficiency: from fatal rhabdomyolysis to..:

Kahraman, Ayca Burcu ; Karakaya, Bekir ; Yıldız, Yılmaz...
Neuromuscular Disorders.  32 (2022)  11-12 - p. 931-934 , 2022
Link: https://doi.org/10.1016/..
 
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9

New-Onset Ocular Myasthenia after Multisystem Inflammatory ..:

Yavuz, Pınar ; Demir, Osman Oguz ; Ozsurekci, Yasemin...
The Journal of Pediatrics.  245 (2022)  - p. 213-216 , 2022
Link: https://doi.org/10.1016/..
 
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10

Neonatal presentations of neuromuscular disorders:

Haliloglu, Goknur
European Journal of Paediatric Neurology.  38 (2022)  - p. A6-A11 , 2022
Link: https://doi.org/10.1016/..
 
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11

Evaluation of a girl with 16p13.11 microduplication syndrom..:

Fidan, Hande ; Kerem Mintaze, Günel ; Haliloğlu, Göknur..
Sanamed.  17 (2022)  3 - p. 189-193 , 2022
Link: https://doi.org/10.5937/..
 
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12

Evaluation of changes in physician behavior after introduct..:

Akcan Yildiz, Leman ; Haliloglu, Goknur ; Yalnizoglu, Dilek...
The American Journal of Emergency Medicine.  55 (2022)  - p. 57-63 , 2022
Link: https://doi.org/10.1016/..
 
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13

Managing CLN2 disease: a treatable neurodegenerative condit..:

Mazurkiewicz-Bełdzińska, Maria ; del Toro, Mireia ; Haliloğlu, Göknur...
Expert Review of Neurotherapeutics.  21 (2021)  11 - p. 1275-1282 , 2021
Link: https://doi.org/10.1080/..
 
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14

Further expanding the mutational spectrum of brain abnormal..:

Kındış, Erdem ; Simsek‐Kiper, Pelin Özlem ; Koşukcu, Can...
American Journal of Medical Genetics Part A.  185 (2021)  6 - p. 1888-1896 , 2021
Link: https://doi.org/10.1002/..
 
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15

Natural history of TRPV4-Related disorders: From skeletal d..:

Ürel-Demir, Gizem ; Şimşek-Kiper, Pelin Özlem ; Öncel, İbrahim...
European Journal of Paediatric Neurology.  32 (2021)  - p. 46-55 , 2021
Link: https://doi.org/10.1016/..
 
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