Reviewer Acknowledgment
The Editors and Publisher of the Journal of Pediatric Endocrinology and Metabolism would like to thank the members of the Editorial Board and the colleagues listed below for their support in reviewing articles submitted to the journal in 2024. Together with our Editorial Board members, our reviewers form the backbone of JPEM: they ensure the consistently high quality of the publications in this journal.[*]
Abdullah, Mohamed
Acar, Sezer
Agarwal, Gaurav
Ahmad, Ayesha
Ahmad, Noman
Akar, Halil Tuna
Akçay, Teoman
Akin, Mustafa Ali
Akin, Mustafa Senol
Alavi, Afagh
Andrade, Nathalia
Anık, Ahmet
Arisaka, Osamu
Arman, Ahmet
Assirelli, Valentina
Atabek, Mehmet Emre
Audí, Laura
Ayesha, Hina
Babiker, Amir
Backeljauw, Philippe
Balcı, Mehmet
Batista Lemes, Vanilson
Bechtold-Dalla Pozza, Susanne
Becker, Marianne
Bertelloni, Silvano
Beser Ozmen, Esra
Bettendorf, Markus
Biester, Torben
Binder, Gerhard
Birkebaek, Niels
Blanco, Cynthia
Blau, Nenad
Blom, Dirk J.
Bober, Ece
Boettcher, Claudia
Boggs, Elizabeth
Bowman, Pamela
Bozaci, Ayse Ergul
Brar, Preneet
Brusgaard, Klaus
Bulut, Fatma Derya
Burckhardt, Marie-Anne
Burnett, John
Buyukyilmaz, Gonul
Cacheiro, Pilar
Calabria, Andrew
Calazans, Camila
Camtosun, Emine
Canda, Ebru
Cao, Bingyan
Capatina, Cristina
Carona, Carlos
Castaldi, Biagio
Castellanos, Luz
Castro, Sebastian
Cayir, Atilla
Ceran, Burak
Cetinkaya, Semra
Chaplin, John Eric
Chen, Hua
Chiovato, Luca
Choong, Catherine
Christin-Maitre, Sophie
Cimbek, Emine Ayça
Crock, Patricia
Dağdeviren Çakır, Aydilek
Dalili, Setila
Darendeliler, Feyza
Dateki, Sumito
de Mello, Elza
Delvecchio, Maurizio
Demirbaş Çakıcı, Didem
Demirbilek, Huseyin
d’Hulst, Simon
di Lazzaro, Maria Valeria
Donaldson, Malcolm
Doneray, Hakan
Dorum, Sevil
Durmaz, Erdem
Eckert, Alexander
Elbayiyev, Sarkhan
Erbas, Ibrahim Mert
Eren, Erdal
Ernst, Gundula
Evin, Ferda
Evliyaoglu, Olcay
Fabbri-Scallet, Helena
Fava, Cristiano
Fayed, Hanan Mahmoud
Finken, Martijn J.J.
Finn, Bryan
Finsterer, Josef
Foster, Timothy
Galderisi, Alfonso
Giannakopoulos, Aristeidis
Giannini, Cosimo
Gokcay, Gulden
Goyal, Alpesh
Gravholt, Claus
Grob, Francisca
Groeschel, Samuel
Gunes, Sezgin
Guo, Shicheng
Guran, Tulay
Gurbuz, Fatih
Hadi, Amir
Hadj Kacem, Hassen
Hagen, Casper
Hahn, Andreas
Hammersen, Johanna
Hamza, Rasha
Hannan, Fadil
Hasegawa, Kosei
Hasegawa, Tomonobu
Hashemi Dehkordi, Elham
Hassan, Sara
Hawkes, Colin P.
He, Wen
Herlin, Morten Krogh
Hiort, Olaf
Hoffman, Robert
Holder, Martin
Holick, Michael F.
Holl, Reinhard
Holmboe, Stine
Holmes-Walker, Jane
Höppner, Jakob
Hull, Sarah
Hussain, Khalid
Iafusco, Dario
Ilgaz, Fatma
Ilonen, Jorma
Iughetti, Lorenzo
Jalaludin, Muhammad Yazid
Januś, Dominika
Jarocka-Cyrta, Elzbieta
Jaruratanasirikul, Somchit
Javer, Amin
Kanner, Lauren
Kapellen, Thomas
Kaplowitz, Paul
Kara, Cengiz
Karadag, Nilgun
Karaman, Erbil
Karges, Beate
Kelsey , Megan
Keskin, Mehmet
Keskin, Meliksah
Kettunen, Jarno
Khadilkar, Anuradha
kılavuz, sebile
Kiliç Yildirim, Gonca
Kilic, Mustafa
Kim, Jaehyun
Koca, Serkan
Kochi, Cristiane
Kocova, Mirjana
Kör, Deniz
Kose, Engin
Kottler, Marie-Laure
Kozanoglu, Tugba
Kratzsch, Juergen
Kumru Akin, Burcu
Lahoti, Amit
Lakmini, Balagamage
Lal, Sadhna Bhasin
Lalayiannis, Alexander
Larsson, Helena Elding
Law, James
Le, Nguyen Quoc Khanh
Lebl, Jan
Lee , Ji Eun
Lee, Kee-Hyoung
Lewinski, Andrzej
Liao, Xiang-Peng
Liimatta, Jani
Lipay, Monica V.
Liu, Qin
Lodish, Maya
Lucas-Herald, Angela
Luo, Xiaoping
Lyra, Maria Julia
Maffeis, Claudio
Malaquias, A.
Mamilly, L
Manoli, Irini
Marwaha, Raman
Mazeh, Haggi
McElreavey, Kenneth
Michigami, Toshimi
Mill, José Geraldo
Minamitani, Kanshi
Mittelman, Steven
Mohamed, Zainaba
Mooij, Christiaan
Morabito, Letteria Anna
Müller, Hermann
Nagasaki, Keisuke
Nakajima, Hisakazu
Nakamura, Chizuko
Neumann, Uta
Ng, Nicholas Beng Hui
Niedziela, Marek
Nittari, Giulio
Nybo, Mads
Okur, Ilyas
Olgaç, Asburçe
Osganian, Stavroula K.
Ozbek, Mehmet
Özcabı, Bahar
Ozen, Samim
Özkan, Behzat
Ozsu, Elif
Paisey, R.B.
Palany, Raghupathy
Panda, Santosh Kumar
Parlak, Mesut
Pavone, Piero
Pawelczak, Melissa
Pei, Zhou
Piovesan, Alessandro
Pirgon, Ozgur
Potorac, Iulia
Poulain, Tanja
Poyrazoglu, Sukran
Procianoy, Renato
Quinzii, Catarina
Radetti, Giorgio
Raff, Hershel
Rai, Preeti
Rasmussen, Nicklas
Rathish, D.
Ravio, Taneli
Reschke, Felix
Rey, Rodolfo
Rezende, Raissa
Roohani, Mohammad
Rosenbauer, Joachim
Sachdev, Pooja
Salas, Ariel A.
Salerno, Mariacarolina
Santana-da-Silva, Luiz
Sass, Joern
Savage, Martin
Sawant, Sangeeta Priyadarshi
Schumann, Anke
Schwahn, Bernd
Schweizer, Roland
Schwimmer, J.B.
Selver Eklioglu, Beray
Shah, Nikhil
Shi, Yufei
Shkalim Zemer, Vered
Siklar, Zeynep
Stahl-Pehe, Anna
Stepien, Karolina
Stratakis, Constantine A.
Streisand, Randi
Tadiotto, Maiara
Taketani, T.
Tall, Susanna
Tatsuhiko, Urakami
Tekin, Mehmet
Ting, Tzer Hwu
Topaloğlu, Ali
Topaloglu, Rezan
Torchen, Laura
Toumba, Meropi
Treglia, Giorgio
Tsai, Meng-Che
Tseretopoulou, Xanthippi
Tuğcu, Ali
Tung, Joanna
Tutunculer, Filiz
Uday, Suma
Umpaichitra, Vatcharapan
Ünal Uzun, Özlem
Unal, Edip
Villares, Maria
Völkl, Thomas
Wagdy, Reham M.
Wang, Xiumin
Ward, Leigh
Wasniewska, Malgorzata
Wassermann, Jonathan
Wiegand, Susanna
Winner, Kay
Witchel, Selma
Wolf, B.
Wolf, Nicole
Wolf, Risa
Wolfsdorf, Joseph I.
Wood, Claire
Yang, Lin
Yesiltepe Mutlu, Gul
Yildiz, Duran
Yıldız, Yılmaz
Zemel, Babette
Zeng, Baoqi
Zevin, Erika
Zhang, Hao
Zhang, Zhaoyun
Zhao, Qu-ming
Zubarioglu, Tanyel
© 2024 Walter de Gruyter GmbH, Berlin/Boston
Articles in the same Issue
- Frontmatter
- Review
- Effect and safety of aromatase inhibitors for the treatment of short stature in male children and adolescents: a meta-analysis of randomized controlled trials
- Original Articles
- Do hybrid closed loop insulin pump systems improve glycemic control and reduce hospitalizations in poorly controlled type 1 diabetes?
- Long-term effectiveness and safety of long-acting growth hormone preparation in children with growth hormone deficiency
- Gonadal changes in children and adolescents with congenital adrenal hyperplasia
- Hsa_circ_0002473 inhibits GH3 cell proliferation and GH secretion as a competitive endogenous RNA for has-miR-4645-3p
- Through the eyes of the parents: a transdiagnostic psychiatric perspective for children with differences of sexual development
- Experiences and psychological issues affecting parents of children born with atypical genitalia in India
- Case Reports
- A rare case of central precocious puberty in a male infant with adrenal hypoplasia congenita
- Gly183Ser homozygous mutation of the steroid 5-a reductase type 2 (SRD5A2) gene in a Brazilian patient: case report
- Novel PIK3R1 gene mutation associated with SHORT syndrome: a case report of a 15-year-old female
- Mineralocorticoid receptor antagonist monotherapy in pediatric non-classical 11β-hydroxylase deficiency
- A rare case of skeletal dysplasia: biallelic variant in ACAN gene
- Letter to the Editor
- Another look at the necessity of polysomnography for infants with Prader-Willi syndrome prior to initiation of growth hormone therapy
- Annual Reviewer Acknowledgment
- Reviewer Acknowledgment
Articles in the same Issue
- Frontmatter
- Review
- Effect and safety of aromatase inhibitors for the treatment of short stature in male children and adolescents: a meta-analysis of randomized controlled trials
- Original Articles
- Do hybrid closed loop insulin pump systems improve glycemic control and reduce hospitalizations in poorly controlled type 1 diabetes?
- Long-term effectiveness and safety of long-acting growth hormone preparation in children with growth hormone deficiency
- Gonadal changes in children and adolescents with congenital adrenal hyperplasia
- Hsa_circ_0002473 inhibits GH3 cell proliferation and GH secretion as a competitive endogenous RNA for has-miR-4645-3p
- Through the eyes of the parents: a transdiagnostic psychiatric perspective for children with differences of sexual development
- Experiences and psychological issues affecting parents of children born with atypical genitalia in India
- Case Reports
- A rare case of central precocious puberty in a male infant with adrenal hypoplasia congenita
- Gly183Ser homozygous mutation of the steroid 5-a reductase type 2 (SRD5A2) gene in a Brazilian patient: case report
- Novel PIK3R1 gene mutation associated with SHORT syndrome: a case report of a 15-year-old female
- Mineralocorticoid receptor antagonist monotherapy in pediatric non-classical 11β-hydroxylase deficiency
- A rare case of skeletal dysplasia: biallelic variant in ACAN gene
- Letter to the Editor
- Another look at the necessity of polysomnography for infants with Prader-Willi syndrome prior to initiation of growth hormone therapy
- Annual Reviewer Acknowledgment
- Reviewer Acknowledgment