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Delayed Adrenarche may be an Additional Feature of Immunoglobulin Super Family Member 1 Deficiency Syndrome
Delayed Adrenarche may be an Additional Feature of Immunoglobulin Super Family Member 1 Deficiency Syndrome
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Delayed Adrenarche may be an Additional Feature of Immunoglobulin Super Family Member 1 Deficiency Syndrome

Van Hulle, Severine ; Craen, Margarita ; Callewaert, Bert ; Joustra, Sjoerd ; Oostdijk, Wilma ; Losekoot, Monique ; Wit, Jan Maarten ; Turgeon, Marc Olivier ; Bernard, Daniel J ; De Schepper, Jean

Journal of clinical research in pediatric endocrinology, 2016-03, Vol.8 (1), p.86-91 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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2
Lumbar Spinal Stenosis: A Rare Presentation of Hereditary Transthyretin Amyloidosis
Lumbar Spinal Stenosis: A Rare Presentation of Hereditary Transthyretin Amyloidosis
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Lumbar Spinal Stenosis: A Rare Presentation of Hereditary Transthyretin Amyloidosis

Çakar, Arman ; Atmaca, Murat Mert ; Kotan, Dilcan ; Durmuş, Hacer ; Deymeer, Feza ; Oflazer, Piraye ; Parman, Yeşim

Noro-Psikiyatri Arsivi, 2022-03, Vol.59 (1), p.77-79 [Periódico revisado por pares]

Turkey: AVES

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3
A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family
A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family
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A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family

Dursun, Fatma ; Mohamoud, Hussein Sheikh Ali ; Karim, Noreen ; Naeem, Muhammad ; Jelani, Musharraf ; Kırmızıbekmez, Heves

Journal of clinical research in pediatric endocrinology, 2016-12, Vol.8 (4), p.472-477 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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4
Complete Penile Duplication with Structurally Normal Penises: A Case Report
Complete Penile Duplication with Structurally Normal Penises: A Case Report
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Complete Penile Duplication with Structurally Normal Penises: A Case Report

Akgul, Ahsen Karagozlu ; Ucar, Murat ; Celik, Fatih ; Kiristioglu, Irfan ; Kilic, Nizamettin Koçak,Zafer

Balkan medical journal, 2018-08, Vol.35 (4), p.340-343 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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5
Rare Fibroepithelial Polyp Extending Along the Ureter: A Case Report
Rare Fibroepithelial Polyp Extending Along the Ureter: A Case Report
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Rare Fibroepithelial Polyp Extending Along the Ureter: A Case Report

Akdere, Hakan ; Çevik, Gökhan Koçak,Zafer

Balkan medical journal, 2018-05, Vol.35 (3), p.275-277 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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6
Successful Management of Aggressive Fibromatosis of the Neck: A Case Report
Successful Management of Aggressive Fibromatosis of the Neck: A Case Report
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Successful Management of Aggressive Fibromatosis of the Neck: A Case Report

Avinçsal, Özgür Mehmet ; Shinomiya, Hirotaka ; Otsuki, Naoki ; Sasaki, Ryohei ; Nibu, Ken-ichi Koçak,Zafer

Balkan medical journal, 2018-05, Vol.35 (3), p.278-281 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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7
A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene
A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene
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A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene

Keskin, Melikşah ; Muratoğlu Şahin, Nursel ; Kurnaz, Erdal ; Bayramoğlu, Elvan ; Savaş Erdeve, Şenay ; Aycan, Zehra ; Çetinkaya, Semra Darendeliler,Fatma Feyza

Journal of clinical research in pediatric endocrinology, 2017-03, Vol.9 (1), p.91-94 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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8
Phenotypic Variability in a Family with Acrodysostosis Type 2 Caused by a Novel PDE4D Mutation Affecting the Serine Target of Protein Kinase-A Phosphorylation
Phenotypic Variability in a Family with Acrodysostosis Type 2 Caused by a Novel PDE4D Mutation Affecting the Serine Target of Protein Kinase-A Phosphorylation
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Phenotypic Variability in a Family with Acrodysostosis Type 2 Caused by a Novel PDE4D Mutation Affecting the Serine Target of Protein Kinase-A Phosphorylation

Hoppmann, Julia ; Gesing, Julia ; Silve, Caroline ; Leroy, Chrystel ; Bertsche, Astrid ; Hirsch, Franz Wolfgang ; Kiess, Wieland ; Pfäffle, Roland ; Schuster, Volker Darendeliler,Fatma Feyza

Journal of clinical research in pediatric endocrinology, 2017-12, Vol.9 (4), p.360-365 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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9
Urothelial Carcinoma of the Bladder in Pediatric Patient: Four Case Series and Review of the Literature
Urothelial Carcinoma of the Bladder in Pediatric Patient: Four Case Series and Review of the Literature
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Urothelial Carcinoma of the Bladder in Pediatric Patient: Four Case Series and Review of the Literature

Uçar, Murat ; Demirkaya, Metin ; Aytaç Vuruşkan, Berna ; Balkan, Emin ; Kılıç, Nizamettin Koçak,Zafer

Balkan medical journal, 2018-05, Vol.35 (3), p.268-271 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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10
Congenital Superior Sternal Cleft Repair Using Primary Closure
Congenital Superior Sternal Cleft Repair Using Primary Closure
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Congenital Superior Sternal Cleft Repair Using Primary Closure

Karamustafaoglu, Yekta Altemur ; Yanik, Fazli ; Yoruk, Yener ; Basaran, Umit Nusret Koçak,Zafer

Balkan medical journal, 2019-03, Vol.36 (2), p.141-142 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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