Mehmet Keskin (M Keskin)

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 9

Top Topics

Pulmonary Embolism

Psychometric Properties

Top Venues

European journal of pediatrics

Journal of endocrinological investigation

Journal of clinical research in pediatric endocrinology

Journal of pediatric endocrinology & metabolism : JPEM

This page only lists publications with an associated author ORCID identifier.

Publications

Murat Karaoglan, Gulper Nacarkahya, Emel Hatun Aytac, Mehmet Keskin
Genotype and clinical phenotype of children with Marfan syndrome in Southeastern Anatolia. European journal of pediatrics 183 (8) (2024)
Murat Karaoglan, Gulper Nacarkahya, Emel Hatun Aytac, Mehmet Keskin
Genotype and clinical phenotype of children with Marfan syndrome in Southeastern Anatolia. European journal of pediatrics 183 (8) (2024)
Elif Arık, Özlem Keskin, Serpil Albayrak, Mehmet Keskin, Mahmut Cesur, Murat Karaoglan, Gaye Inal, Ahmet Yildirim, Ercan Kucukosmanoglu
Allergic reactions to enzyme replacement therapy in children with lysosomal storage diseases and their management. Journal of pediatric endocrinology & metabolism : JPEM (2024)
Y Özer, Ahmet Anik, Uğurcan Sayılı, U Tercan, Reyhan Deveci Sevim, Sebla Güneş, M Buhur Pirimoğlu, Selin Elmaoğulları, İsmail Dündar, Deniz Ökdemir, Özge Besci, Arzu Jalilova, D Çiçek, B Singin, Ş E Ulu, Hande Turan, Serpil Albayrak, Zümrüt Kocabey Sütçü, Beray Selver Eklioğlu, Erdal Eren, Semra Cetinkaya, Senay Savas Erdeve, İhsan Esen, Korcan Demir, Şükran Darcan, Nihal Hatipoglu, Mesut Parlak, Fatma Dursun, Zeynep Şiklar, Merih Berberoğlu, Mehmet Keskin, Zerrin Orbak, Başak Tezel, E Yürüker, Bekir Keskinkilic, Fatih Kara, Ethem Erginoz, Feyza Darendelıler, Saadet Olcay Evliyaoglu
High frequency of transient congenital hypothyroidism among infants referred for suspected congenital hypothyroidism from the Turkish National screening program: thyroxine dose may guide the prediction of transients. Journal of endocrinological investigation (2024)
Y Özer, Ahmet Anik, Uğurcan Sayılı, U Tercan, Reyhan Deveci Sevim, Sebla Güneş, M Buhur Pirimoğlu, Selin Elmaoğulları, İsmail Dündar, Deniz Ökdemir, Özge Besci, Arzu Jalilova, D Çiçek, B Singin, Ş E Ulu, Hande Turan, Serpil Albayrak, Zümrüt Kocabey Sütçü, Beray Selver Eklioğlu, Erdal Eren, Semra Cetinkaya, Senay Savas Erdeve, İhsan Esen, Korcan Demir, Şükran Darcan, Nihal Hatipoglu, Mesut Parlak, Fatma Dursun, Zeynep Şiklar, Merih Berberoğlu, Mehmet Keskin, Zerrin Orbak, Başak Tezel, E Yürüker, Bekir Keskinkilic, Fatih Kara, Ethem Erginoz, Feyza Darendelıler, Saadet Olcay Evliyaoglu
High frequency of transient congenital hypothyroidism among infants referred for suspected congenital hypothyroidism from the Turkish National screening program: thyroxine dose may guide the prediction of transients. Journal of endocrinological investigation 47 (9) (2024)
Murat Karaoglan, Gulper Nacarkahya, Emel Hatun Aytac, Mehmet Keskin
Genotype and clinical phenotype of children with Marfan syndrome in Southeastern Anatolia. European journal of pediatrics (2024)
Murat Karaoglan, Gulper Nacarkahya, Emel Hatun Aytac, Mehmet Keskin
Genotype and clinical phenotype of children with Marfan syndrome in Southeastern Anatolia. European journal of pediatrics 183 (8) (2024)
Murat Karaoglan, Gulper Nacarkahya, Mehmet Keskin, Özlem Keskin
Immunophenotypic analysis of lymphocyte subsets in newborns with biotinidase deficiency. Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology 32 (3) (2020)
Tülay Güran, Başak Tezel, Meltem Çakır, Ayşehan Akıncı, Zerrin Orbak, Mehmet Keskin, Beray Selver Eklioğlu, Zeynep Alev Ozon, Mehmet Nuri Özbek, Gülay Karagüzel, Nihal Hatipoglu, Fatih Gurbuz, Filiz Mine Çizmecioğlu-Jones, Cengiz Kara, Enver Şimşek, Firdevs Baş, Hasan Murat Aydın, Feyza Darendelıler
Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: Outcomes of Extended Pilot Study in 241,083 Infants Journal of clinical research in pediatric endocrinology 12 (3) (2020)