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Muhsin Elmas
Assoc. Prof. Dr.
istanbul eğitim ve araştırma hastanesi
Publication
8
Review
15
CrossRef Cited
3
8
Publication
15
Review
3
CrossRef Cited
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Summary
Publications
Peer Review
Cited
Research Fields
Epigenetics
Gene Mapping
Developmental Genetics
Health Sciences
Institution
istanbul eğitim ve araştırma hastanesi
Publications
Is rheumatoid arthritis a neglected comorbidity in neurofibromatosis type 1?
Authors:
Adem Erturk
,
Alper Sarı
,
Ali İzzet Akçin
,
Ali Sadri Uysal
,
Muhsin Elmas
,
Çağrı Turan
Published: 2023 ,
Journal of Health Sciences and Medicine
DOI: 10.32322/jhsm.1310764
FAVORITE
0
TOTAL DOWNLOAD COUNT
566
0
FAVORITE
566
TOTAL DOWNLOAD COUNT
ORAL AND DENTAL FINDINGS OF A CHILD WITH WEILL-MARCHESANI SYNDROME TYPE II: A CASE REPORT WITH 3-YEAR FOLLOW-UP
Authors:
Burcu Güçyetmez Topal
,
Muhsin Elmas
,
Melike Tıraş
Published: 2023 ,
Selcuk Dental Journal
DOI: 10.15311/selcukdentj.1231513
FAVORITE
0
TOTAL DOWNLOAD COUNT
501
0
FAVORITE
501
TOTAL DOWNLOAD COUNT
Genetic and Clinical Evaluation of Retinitis Pigmentosa
Authors:
Özgür Eroğul
,
Muhsin Elmas
,
Mustafa Doğan
,
Hamidu Hamisi Gobeka
,
Ayça Nur Demir
,
Leyla Eryiğit Eroğul
Published: 2022 ,
Journal of Contemporary Medicine
DOI: 10.16899/jcm.1131536
FAVORITE
0
TOTAL DOWNLOAD COUNT
1329
0
FAVORITE
1329
TOTAL DOWNLOAD COUNT
A CASE OF PEBAT SYNDROME WITH A NOVEL MUTATION IN TUBULIN-SPECIFIC CHAPERONE D (TBCD) GENE
Authors:
Muhsin Elmas
, Başak Göğüş,
Ayşegül Bükülmez
,
Mustafa Solak
Published: 2022 ,
Kocatepe Medical Journal
DOI: 10.18229/kocatepetip.471957
FAVORITE
0
TOTAL DOWNLOAD COUNT
1534
0
FAVORITE
1534
TOTAL DOWNLOAD COUNT
The road from mutation to next generation phenotyping: contribution of deep learning technology (Face2Gene) to diagnosis neurofibromatosis type 1
Authors:
Muhsin Elmas
,
Başak Göğüş
Published: 2022 ,
The European Research Journal
DOI: 10.18621/eurj.894631
FAVORITE
0
TOTAL DOWNLOAD COUNT
835
0
FAVORITE
835
TOTAL DOWNLOAD COUNT
EVALUATION OF DEMOGRAPHIC, CLINICAL, LABORATORY AND GENETIC CHARACTERISTICS OF CHILDREN WITH FAMILIAL MEDITERRANEAN FEVER IN AFYONKARAHİSAR REGION
Authors:
Ebru Elmas
,
Ayşegül Bükülmez
,
Muhsin Elmas
,
Gülay Demircin
Published: 2021 ,
Kocatepe Medical Journal
DOI: 10.18229/kocatepetip.690148
FAVORITE
0
TOTAL DOWNLOAD COUNT
664
0
FAVORITE
664
TOTAL DOWNLOAD COUNT
PRENATAL FINDINGS IN DOWN SYNDROME CASES
Authors:
Muhsin Elmas
Published: 2021 ,
Kocatepe Medical Journal
DOI: 10.18229/kocatepetip.689070
FAVORITE
0
TOTAL DOWNLOAD COUNT
3248
0
FAVORITE
3248
TOTAL DOWNLOAD COUNT
THE INVESTIGATION OF JOINT HYPERMOBILITY, QUALITY OF LIFE AND SOCIODEMOGRAPHIC DATA OF PERSONS WHO HAVE OBTAINED SPORTS TRAINING: PROSPECTIVE RANDOMIZED CONTROLLED STUDY
Authors:
Muhsin Elmas
, Başak Gogus,
Yücel Ocak
Published: 2020 ,
Acta Medica Nicomedia
DOI: -
FAVORITE
0
TOTAL DOWNLOAD COUNT
1286
0
FAVORITE
1286
TOTAL DOWNLOAD COUNT
Articles published in
Acta Medica Nicomedia
Journal of Contemporary Medicine
Journal of Health Sciences and Medicine
Kocatepe Medical Journal
Selcuk Dental Journal
The European Research Journal
Reviews
Anatolian Journal of Botany
Celal Bayar Üniversitesi Sağlık Bilimleri Enstitüsü Dergisi
Journal of Biotechnology and Strategic Health Research
Journal of Contemporary Medicine
Journal of Duzce University Health Sciences Institute
Kocatepe Medical Journal
Konuralp Medical Journal
Sağlıkta Performans ve Kalite Dergisi
Value in Health Sciences
Publications
Genetic and Clinical Evaluation of Retinitis Pigmentosa
Authors:
Özgür Eroğul
,
Muhsin Elmas
,
Mustafa Doğan
,
Hamidu Hamisi Gobeka
,
Ayça Nur Demir
,
Leyla Eryiğit Eroğul
Published: 2022 ,
Journal of Contemporary Medicine
DOI: 10.16899/jcm.1131536
CITED
1
FAVORITE
0
TOTAL DOWNLOAD COUNT
1329
1
CITED
0
FAVORITE
1329
TOTAL DOWNLOAD COUNT
A CASE OF PEBAT SYNDROME WITH A NOVEL MUTATION IN TUBULIN-SPECIFIC CHAPERONE D (TBCD) GENE
Authors:
Muhsin Elmas
, Başak Göğüş,
Ayşegül Bükülmez
,
Mustafa Solak
Published: 2022 ,
Kocatepe Medical Journal
DOI: 10.18229/kocatepetip.471957
CITED
1
FAVORITE
0
TOTAL DOWNLOAD COUNT
1534
1
CITED
0
FAVORITE
1534
TOTAL DOWNLOAD COUNT
The road from mutation to next generation phenotyping: contribution of deep learning technology (Face2Gene) to diagnosis neurofibromatosis type 1
Authors:
Muhsin Elmas
,
Başak Göğüş
Published: 2022 ,
The European Research Journal
DOI: 10.18621/eurj.894631
CITED
1
FAVORITE
0
TOTAL DOWNLOAD COUNT
835
1
CITED
0
FAVORITE
835
TOTAL DOWNLOAD COUNT