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Items: 1 to 20 of 27

1.

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.

2.

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
3.

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.

4.

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
5.

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.

6.

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.

7.

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.

8.

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
9.

Birthweight Differences in Monozygotic Twins Influence Pubertal Maturation and Near Final Height.

Schulte S, Wölfle J, Schreiner F, Stoffel-Wagner B, Peter M, Bartmann P, Gohlke B.

J Pediatr. 2016 Mar;170:288-94.e1-2. doi: 10.1016/j.jpeds.2015.12.020. Epub 2016 Jan 12.

PMID:
26794471
10.

Infancy-Onset T1DM, Short Stature, and Severe Immunodysregulation in Two Siblings With a Homozygous LRBA Mutation.

Schreiner F, Plamper M, Dueker G, Schoenberger S, Gámez-Díaz L, Grimbacher B, Hilger AC, Gohlke B, Reutter H, Woelfle J.

J Clin Endocrinol Metab. 2016 Mar;101(3):898-904. doi: 10.1210/jc.2015-3382. Epub 2016 Jan 8.

PMID:
26745254
11.

DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations.

Sharma A, Jamil MA, Nuesgen N, Schreiner F, Priebe L, Hoffmann P, Herns S, Nöthen MM, Fröhlich H, Oldenburg J, Woelfle J, El-Maarri O.

Clin Epigenetics. 2015 Jul 28;7:76. doi: 10.1186/s13148-015-0112-2. eCollection 2015.

12.

Genetic variants of the vitamin K dependent coagulation system and intraventricular hemorrhage in preterm infants.

Schreiner C, Suter S, Watzka M, Hertfelder HJ, Schreiner F, Oldenburg J, Bartmann P, Heep A.

BMC Pediatr. 2014 Sep 1;14:219. doi: 10.1186/1471-2431-14-219.

13.

MKRN3 mutations in familial central precocious puberty.

Schreiner F, Gohlke B, Hamm M, Korsch E, Woelfle J.

Horm Res Paediatr. 2014;82(2):122-6. doi: 10.1159/000362815. Epub 2014 Jul 5.

PMID:
25011910
14.

11p15 DNA-methylation analysis in monozygotic twins with discordant intrauterine development due to severe twin-to-twin transfusion syndrome.

Schreiner F, Gohlke B, Stutte S, Bartmann P, Hecher K, Oldenburg J, El-Maarri O, Woelfle J.

Clin Epigenetics. 2014 Mar 28;6(1):6. doi: 10.1186/1868-7083-6-6.

15.

Novel acid-labile subunit ( IGFALS ) mutation p.T145K (c.434C>A) in a patient with ALS deficiency, normal stature and immunological dysfunction.

Schreiner F, Schoenberger S, Koester B, Domené HM, Woelfle J.

Horm Res Paediatr. 2013;80(6):424-30. doi: 10.1159/000355927. Epub 2013 Nov 27.

PMID:
24296365
16.

Postnatal nutrition in extremely low birth weight infants and its impact on growth until the age of 6 years.

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

Acta Paediatr. 2014 Feb;103(2):e61-8. doi: 10.1111/apa.12469. Epub 2013 Dec 3.

PMID:
24127881
17.

Methylation of L1Hs promoters is lower on the inactive X, has a tendency of being higher on autosomes in smaller genomes and shows inter-individual variability at some loci.

Singer H, Walier M, Nüsgen N, Meesters C, Schreiner F, Woelfle J, Fimmers R, Wienker T, Kalscheuer VM, Becker T, Schwaab R, Oldenburg J, El-Maarri O.

Hum Mol Genet. 2012 Jan 1;21(1):219-35. doi: 10.1093/hmg/ddr456. Epub 2011 Oct 4.

18.

Association of COMT genotypes with S-COMT promoter methylation in growth-discordant monozygotic twins and healthy adults.

Schreiner F, El-Maarri O, Gohlke B, Stutte S, Nuesgen N, Mattheisen M, Fimmers R, Bartmann P, Oldenburg J, Woelfle J.

BMC Med Genet. 2011 Sep 1;12:115. doi: 10.1186/1471-2350-12-115.

19.

Insulin-like growth factor-I in cord blood is predictive of catch-up growth in monozygotic twins with discordant growth.

Gohlke BC, Schreiner F, Fimmers R, Bartmann P, Woelfle J.

J Clin Endocrinol Metab. 2010 Dec;95(12):5375-81. doi: 10.1210/jc.2010-0271. Epub 2010 Sep 1.

PMID:
20810576
20.

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