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Turk Patoloji Dergisi
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January 12, 2021
The Histopathologic Examination of a Second Muscle Biopsy Specimen at a Later Date may Sometimes be the Best Approach to Make a Differential Diagnosis in Neuromuscular Disorders
Gulden Diniz, Berk Ozyilmaz, Sarenur Gokben
Medeniyet Medical Journal
|
August 22, 2020
Heterozygous Beta Chain Variant Hemoglobin Pusan: A Rare Case Report in Turkish Population
Durmus Ayan, Ozgur Kirbiyik, Berk Ozyilmaz
International Journal of Clinical Practice
|
November 17, 2020
JAK2V617F, CALR and MPL515L/K mutations and plateletcrit in essential thrombocythemia: A single centre's experience
Cengiz Ceylan, Berk Ozyilmaz, Ozgur Kirbiyik, et al.
Acta Neurologica Belgica
|
June 27, 2019
A hypomyelinating leukodystrophy with calcification: oculodentodigital dysplasia
Dilek Cavusoglu, Nihal Olgac Dundar, Pinar Arican, et al.
Journal of Child Neurology
|
August 26, 2025
Beyond the Copy Number Differences: The Phenotypic Diversity of Children With 15q11.2 Microdeletions and Microduplications
Gunce Basarir, Irmak Erdogan, Berk Ozyilmaz, et al.
Indian Journal of Pathology & Microbiology
|
April 18, 2022
ALK, ROS1 and EGFR status of lung cancers in the Aegean Region of Turkey
Gulden Diniz, Berna Komurcuoglu, Berk Ozyilmaz, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
August 7, 2025
Demographic, clinical, and genetic characteristics of patients with Limb-Girdle Muscular Dystrophies (LGMD): A single tertiary-center experience
Murat Yildirim Kale, Huseyin Anil Korkmaz, Berk Ozyilmaz, et al.
Journal of Pediatric Genetics
|
May 1, 2018
A De Novo Xp11.23 Duplication in a Girl with a Severe Phenotype: Expanding the Clinical Spectrum
Pinar Arican, Dilek Cavusoglu, Pinar Gencpinar, et al.
Medicine
|
April 5, 2024
JAKCalc: A machine-learning approach to rationalized JAK2 testing in patients with elevated hemoglobin levels
Fatos Dilan Koseoglu, Fatma Keklik Karadag, Hale Bulbul, et al.
Journal of Pediatric Genetics
|
February 19, 2019
Chromosomal Microarray Analysis in Children with Unexplained Developmental Delay/Intellectual Disability
Pinar Arican, Nihal Olgac Dundar, Berk Ozyilmaz, et al.
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Search research articles
Search
Showing results (1-10 of 23) with videos related to
Sort By:
Page
of 3
Turk Patoloji Dergisi
|
January 12, 2021
The Histopathologic Examination of a Second Muscle Biopsy Specimen at a Later Date may Sometimes be the Best Approach to Make a Differential Diagnosis in Neuromuscular Disorders
Gulden Diniz, Berk Ozyilmaz, Sarenur Gokben
Medeniyet Medical Journal
|
August 22, 2020
Heterozygous Beta Chain Variant Hemoglobin Pusan: A Rare Case Report in Turkish Population
Durmus Ayan, Ozgur Kirbiyik, Berk Ozyilmaz
International Journal of Clinical Practice
|
November 17, 2020
JAK2V617F, CALR and MPL515L/K mutations and plateletcrit in essential thrombocythemia: A single centre's experience
Cengiz Ceylan, Berk Ozyilmaz, Ozgur Kirbiyik, et al.
Acta Neurologica Belgica
|
June 27, 2019
A hypomyelinating leukodystrophy with calcification: oculodentodigital dysplasia
Dilek Cavusoglu, Nihal Olgac Dundar, Pinar Arican, et al.
Journal of Child Neurology
|
August 26, 2025
Beyond the Copy Number Differences: The Phenotypic Diversity of Children With 15q11.2 Microdeletions and Microduplications
Gunce Basarir, Irmak Erdogan, Berk Ozyilmaz, et al.
Indian Journal of Pathology & Microbiology
|
April 18, 2022
ALK, ROS1 and EGFR status of lung cancers in the Aegean Region of Turkey
Gulden Diniz, Berna Komurcuoglu, Berk Ozyilmaz, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
August 7, 2025
Demographic, clinical, and genetic characteristics of patients with Limb-Girdle Muscular Dystrophies (LGMD): A single tertiary-center experience
Murat Yildirim Kale, Huseyin Anil Korkmaz, Berk Ozyilmaz, et al.
Journal of Pediatric Genetics
|
May 1, 2018
A De Novo Xp11.23 Duplication in a Girl with a Severe Phenotype: Expanding the Clinical Spectrum
Pinar Arican, Dilek Cavusoglu, Pinar Gencpinar, et al.
Medicine
|
April 5, 2024
JAKCalc: A machine-learning approach to rationalized JAK2 testing in patients with elevated hemoglobin levels
Fatos Dilan Koseoglu, Fatma Keklik Karadag, Hale Bulbul, et al.
Journal of Pediatric Genetics
|
February 19, 2019
Chromosomal Microarray Analysis in Children with Unexplained Developmental Delay/Intellectual Disability
Pinar Arican, Nihal Olgac Dundar, Berk Ozyilmaz, et al.
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of 3