journal of pediatric endocrinology & metabolism : jpem | Journament

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journal of pediatric endocrinology & metabolism : jpem

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Indexings
ncbi
Short Name j pediatr endocrinol metab
Abbreviated Name j pediatr endocrinol metab
ISSN 2191-0251
Aim and Scope
URL
Author Instructions

Publications Per Year

Recent Articles (13 total)

2020
Identification of two novel variants in GAA underlying infantile-onset Pompe disease in two Pakistani families.
Ullah, Aman;Zubaida, Bibi;Cheema, Huma Arshad;Naeem, Muhammad;
515 views DOI Abstract
2019
The role of vitamin D replacement therapy in serum FGF23 concentration in children with myelomeningocele compared with healthy children - a preliminary study.
Bagińska, Joanna;Liszewska, Alicja;Korzeniecka-Kozerska, Agata;
492 views DOI Abstract
2020
The effect of celiac disease and gluten-free diet on pubertal development: a two-center study.
Bayrak, Nevzat Aykut;Volkan, Burcu;Haliloglu, Belma;Kara, Soner Sertan;Cayir, Atilla;
365 views DOI Abstract
2020
Prevalence of obesity and overweight in Iranian students: a systematic review and meta-analysis.
Sarokhani, Diana;Sarokhani, Mandana;Hasanpour Dehkordi, Ali;Ghanei Gheshlagh, Reza;Fakhri, Moloud;
348 views DOI Abstract
2020
The decision-making levels of urine tetrasaccharide for the diagnosis of Pompe disease in the Turkish population.
Canbay, Erhan;Vural, Melisa;Kalkan Uçar, Sema;Sezer, Ebru Demirel;Karasoy, Hatice;Yüceyar, Ayşe Nur;Çoker, Mahmut;Sözmen, Eser Yildirim;
347 views DOI Abstract
2019
Adiposity and attained height in adolescents: a longitudinal analysis from the LabMed Physical Activity Study.
Rosário, Rafaela;Agostinis-Sobrinho, Cesar;Lopes, Luís;Moreira, Pedro;Padrão, Patrícia;Oliveira, André;Moreira, Carla;Póvoas, Susana;Mota, Jorge;Santos, Rute;
337 views DOI Abstract
2019
Nutrition and medical support during pregnancy and lactation in women with inborn errors of intermediary metabolism disorders (IEMDs).
Manta-Vogli, Penelope D;Schulpis, Kleopatra H;Dotsikas, Yannis;Loukas, Yannis L;
337 views DOI Abstract
2020
Two different missense mutations of PEX genes in two similar patients with severe Zellweger syndrome: an argument on the genotype-phenotype correlation.
Havali, Cengiz;Dorum, Sevil;Akbaş, Yılmaz;Görükmez, Orhan;Hirfanoglu, Tugba;
333 views DOI Abstract
2019
Clinical findings in five Turkish patients with citrin deficiency and identification of a novel mutation on SLC25A13.
Köse, Melis Demir;Kagnici, Mehtap;Özdemir, Taha Reşit;Erdur, Cahit Barış;Erdemir, Gülin;Karakoyun, Miray;Guzin, Yiğit;Ceylaner, Serdar;Genel, Ferah;
299 views DOI Abstract
2019
Can preimplantation genetic diagnosis be used for monogenic endocrine diseases?
Yeager, Stephanie;Mehta, Shilpa;Sodhi, Misha;Shah, Bina;
, pp. 0-0
240 views DOI Abstract
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