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Items: 1 to 20 of 70

1.

Monozygotic Twins with Birth-Weight Differences: Metabolic Health Influenced more by Genetics or by Environment?

Grunewald M, Schulte S, Bartmann P, Stoffel-Wagner B, Fimmers R, Woelfle J, Gohlke B.

Horm Res Paediatr. 2019 Aug 14:1-9. doi: 10.1159/000501775. [Epub ahead of print]

PMID:
31412339
2.

Phenotype-Driven Diagnostic of PTEN Hamartoma Tumor Syndrome: Macrocephaly, But Neither Height nor Weight Development, Is the Important Trait in Children.

Plamper M, Gohlke B, Schreiner F, Woelfle J.

Cancers (Basel). 2019 Jul 11;11(7). pii: E975. doi: 10.3390/cancers11070975.

3.

Thyroid Function in Monozygotic Twins with Intra-twin Birth Weight Differences: A Prospective Longitudinal Cohort Study.

Schulte S, Gohlke B, Schreiner F, Gruenewald M, Fimmers R, Stoffel-Wagner B, Bartmann P, Woelfle J.

J Pediatr. 2019 Aug;211:164-171.e4. doi: 10.1016/j.jpeds.2019.03.041. Epub 2019 May 7.

PMID:
31076228
4.

Vitamin D supplementation after the second year of life: joint position of the Committee on Nutrition, German Society for Pediatric and Adolescent Medicine (DGKJ e.V.), and the German Society for Pediatric Endocrinology and Diabetology (DGKED e.V.).

Reinehr T, Schnabel D, Wabitsch M, Bechtold-Dalla Pozza S, Bührer C, Heidtmann B, Jochum F, Kauth T, Körner A, Mihatsch W, Prell C, Rudloff S, Tittel B, Woelfle J, Zimmer KP, Koletzko B.

Mol Cell Pediatr. 2019 May 6;6(1):3. doi: 10.1186/s40348-019-0090-0.

5.

Frequency and Characteristics of MODY 1 (HNF4A Mutation) and MODY 5 (HNF1B Mutation): Analysis From the DPV Database.

Warncke K, Kummer S, Raile K, Grulich-Henn J, Woelfle J, Steichen E, Prinz N, Holl RW.

J Clin Endocrinol Metab. 2019 Mar 1;104(3):845-855. doi: 10.1210/jc.2018-01696.

PMID:
30535056
6.

Congenital intrahepatic portocaval shunts and hypoglycemia due to secondary hyperinsulinism: a case report and review of the literature.

Weigert A, Bierwolf J, Reutter H, Gembruch U, Woelfle J, Ganschow R, Mueller A.

J Med Case Rep. 2018 Nov 12;12(1):336. doi: 10.1186/s13256-018-1881-y. Review.

7.

Inconsistencies in the management of neonates born to mothers with "thyroid diseases".

Weissenfels PC, Woelfle J, Korsch E, Joergens M, Gohlke B.

Eur J Pediatr. 2018 Nov;177(11):1711-1718. doi: 10.1007/s00431-018-3232-9. Epub 2018 Sep 5.

PMID:
30187120
8.

Sequential measurements of IGF-I serum concentrations in adolescents with Laron syndrome treated with recombinant human IGF-I (rhIGF-I).

Breil T, Kneppo C, Bettendorf M; German IGF-I Deficiency Study Group, Müller HL, Kapelari K, Schnabel D, Woelfle J.

J Pediatr Endocrinol Metab. 2018 Aug 28;31(8):895-902. doi: 10.1515/jpem-2018-0139.

PMID:
29995632
9.

Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany.

Dörr HG, Wollmann HA, Hauffa BP, Woelfle J; German Society of Pediatric Endocrinology and Diabetology.

BMC Endocr Disord. 2018 Jun 8;18(1):37. doi: 10.1186/s12902-018-0263-1.

10.

Mecasermin in Insulin Receptor-Related Severe Insulin Resistance Syndromes: Case Report and Review of the Literature.

Plamper M, Gohlke B, Schreiner F, Woelfle J.

Int J Mol Sci. 2018 Apr 24;19(5). pii: E1268. doi: 10.3390/ijms19051268. Review.

11.

Secular Trends on Birth Parameters, Growth, and Pubertal Timing in Girls with Turner Syndrome.

Woelfle J, Lindberg A, Aydin F, Ong KK, Camacho-Hubner C, Gohlke B.

Front Endocrinol (Lausanne). 2018 Feb 28;9:54. doi: 10.3389/fendo.2018.00054. eCollection 2018.

12.

Thyroid disease in children and adolescents with PTEN hamartoma tumor syndrome (PHTS).

Plamper M, Schreiner F, Gohlke B, Kionke J, Korsch E, Kirkpatrick J, Born M, Aretz S, Woelfle J.

Eur J Pediatr. 2018 Mar;177(3):429-435. doi: 10.1007/s00431-017-3067-9. Epub 2017 Dec 22.

PMID:
29273943
13.

Relationship of Serum Fetuin A with Metabolic and Clinical Parameters in German Children and Adolescents with Type 1 Diabetes.

Reinauer C, Reinehr T, Baechle C, Karges B, Seyfarth J, Foertsch K, Schebek M, Woelfle J, Roden M, Holl RW, Rosenbauer J, Meissner T.

Horm Res Paediatr. 2018;89(2):73-81. doi: 10.1159/000484896. Epub 2017 Dec 5.

PMID:
29207397
14.

Targeted Resequencing of Putative Growth-Related Genes Using Whole Exome Sequencing in Patients with Severe Primary IGF-I Deficiency.

Grosse G, Hilger A, Ludwig M, Reutter H, Lorenzen F, Even G, Holterhus PM, Woelfle J; German GHI Study Group.

Horm Res Paediatr. 2017;88(6):408-417. doi: 10.1159/000480505. Epub 2017 Oct 26.

PMID:
29073591
15.

Lipoprotein-associated phospholipase A2 activity in obese adolescents with and without type 2 diabetes.

Seyfarth J, Reinehr T, Hoyer A, Reinauer C, Bächle C, Karges B, Mayatepek E, Roden M, Hofer SE, Wiegand S, Woelfle J, Kiess W, Rosenbauer J, Holl RW, Meissner T.

J Inherit Metab Dis. 2018 Jan;41(1):73-79. doi: 10.1007/s10545-017-0100-0. Epub 2017 Oct 13.

PMID:
29027597
16.

Developmental programming of somatic growth, behavior and endocannabinoid metabolism by variation of early postnatal nutrition in a cross-fostering mouse model.

Schreiner F, Ackermann M, Michalik M, Hucklenbruch-Rother E, Bilkei-Gorzo A, Racz I, Bindila L, Lutz B, Dötsch J, Zimmer A, Woelfle J.

PLoS One. 2017 Aug 31;12(8):e0182754. doi: 10.1371/journal.pone.0182754. eCollection 2017.

17.

Clinical practice guidelines for the care of girls and women with Turner syndrome: proceedings from the 2016 Cincinnati International Turner Syndrome Meeting.

Gravholt CH, Andersen NH, Conway GS, Dekkers OM, Geffner ME, Klein KO, Lin AE, Mauras N, Quigley CA, Rubin K, Sandberg DE, Sas TCJ, Silberbach M, Söderström-Anttila V, Stochholm K, van Alfen-van derVelden JA, Woelfle J, Backeljauw PF; International Turner Syndrome Consensus Group.

Eur J Endocrinol. 2017 Sep;177(3):G1-G70. doi: 10.1530/EJE-17-0430. Review.

PMID:
28705803
18.

Abstracts of the 52nd Workshop for Pediatric Research : Frankfurt, Germany. 27-28 October 2016.

van den Bruck R, Weil PP, Ziegenhals T, Schreiner P, Juranek S, Gödde D, Vogel S, Schuster F, Orth V, Dörner J, Pembaur D, Röper M, Störkel S, Zirngibl H, Wirth S, Jenke ACW, Postberg J, Boy N, Heringer J, Haege G, Glahn EM, Hoffmann GF, Garbade SF, Burgard P, Kölker S, Chao CM, Yahya F, Moiseenko A, Shrestha A, Ahmadvand N, Quantius J, Wilhelm J, El-Agha E, Zimmer KP, Bellusci S, Staufner C, Kölker S, Prokisch H, Hoffmann GF, Seeliger S, Müller M, Hippe A, Steinkraus H, Wauer R, Lachmann B, Hofmann SR, Hedrich CM, Zierk J, Arzideh F, Haeckel R, Rascher W, Rauh M, Metzler M, Thieme S, Bandoła J, Richter C, Ryser M, Jamal A, Ashton MP, von Bonin M, Kuhn M, Hedrich CM, Bonifacio E, Berner R, Brenner S, Hammersen J, Has C, Naumann-Bartsch N, Stachel D, Kiritsi D, Söder S, Tardieu M, Metzler M, Bruckner-Tuderman L, Schneider H, Bohne F, Langer D, Cencic R, Eggermann T, Zechner U, Pelletier J, Zepp F, Enklaar T, Prawitt D, Pech M, Weckmann M, Heinsen FA, Franke A, Happle C, Dittrich AM, Hansen G, Fuchs O, von Mutius E, Oliver BG, Kopp MV, Paret C, Russo A, Theruvath J, Keller B, El Malki K, Lehmann N, Wingerter A, Neu MA, Aslihan GA, Wagner W, Sommer C, Pietsch T, Seidmann L, Faber J, Schreiner F, Ackermann M, Michalik M, Rother E, Bilkei-Gorzo A, Racz I, Bindila L, Lutz B, Dötsch J, Zimmer A, Woelfle J, Fischer HS, Ullrich TL, Bührer C, Czernik C, Schmalisch G, Stein R, Hofmann SR, Hagenbuchner J, Kiechl-Kohlendorfer U, Obexer P, Ausserlechner MJ, Loges NT, Frommer AT, Wallmeier J, Omran H, Öner-Sieben S, Gimpfl M, Rozman J, Irmler M, Beckers J, De Angelis MH, Roscher A, Wolf E, Ensenauer R, Nemes K, Frühwald M, Hasselblatt M, Siebert R, Kordes U, Kool M, Wang H, Hardy H, Refai O, Barwick KES, Zimmerman HH, Weis J, Baple EL, Crosby AH, Cirak S, Hellmuth C, Uhl O, Standl M, Heinrich J, Thiering E, Koletzko B, Blümel L, Kerl K, Picard D, Frühwald MC, Liebau MC, Reifenberger G, Borkhardt A, Hasselblatt M, Remke M, Tews D, Wabitsch M, Fischer-Posovszky P, Westhoff MA, Nonnenmacher L, Langhans J, Schneele L, Trenkler N, Debatin KM.

Mol Cell Pediatr. 2017 May;4(Suppl 1):5. doi: 10.1186/s40348-017-0071-0. No abstract available.

19.

Impact of Early Nutrition on Body Composition in Children Aged 9.5 Years Born with Extremely Low Birth Weight.

Stutte S, Gohlke B, Peiler A, Schreiner F, Born M, Bartmann P, Woelfle J.

Nutrients. 2017 Feb 10;9(2). pii: E124. doi: 10.3390/nu9020124.

20.

Glucocorticoid Receptor Gene Variants and Neonatal Outcome in Very-Low-Birth-Weight Preterm Infants.

Schreiner C, Schreiner F, Härtel C, Heckmann M, Heep A, Bartmann P, Woelfle J, Müller A, Herting E, Göpel W; German Neonatal Network, GNN.

Neonatology. 2017;111(1):22-29. Epub 2016 Aug 11.

PMID:
27509264

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