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Items: 14

1.

Hepatitis B immune status in adolescents vaccinated during infancy: A retrospective cohort study from a pediatric practice in Germany.

Anderson CL, Remschmidt C, Drobnitzky FP, Falkenhorst G, Zimmermann R, Wichmann O, Harder T.

Hum Vaccin Immunother. 2016 Mar 3;12(3):779-84. doi: 10.1080/21645515.2015.1105414.

2.

Transmission disequilibrium analysis of the functional 5-HT3A receptor variant C178T in early-onset obsessive compulsive-disorder.

Mössner R, Döring N, Scherag A, Schäfer H, Herpertz-Dahlmann B, Remschmidt H, Schulz E, Renner T, Wewetzer C, Warnke A, Lesch KP, Walitza S.

J Psychopharmacol. 2007 Nov;21(8):833-6. Epub 2007 Jan 26.

PMID:
17259209
3.

Serum levels of olanzapine and its N-desmethyl and 2-hydroxymethyl metabolites in child and adolescent psychiatric disorders: effects of dose, diagnosis, age, sex, smoking, and comedication.

Theisen FM, Haberhausen M, Schulz E, Fleischhaker C, Clement HW, Heinzel-Gutenbrunner M, Remschmidt H.

Ther Drug Monit. 2006 Dec;28(6):750-9.

PMID:
17164690
4.

Family-based association study of serotonergic candidate genes and attention-deficit/hyperactivity disorder in a German sample.

Heiser P, Dempfle A, Friedel S, Konrad K, Hinney A, Kiefl H, Walitza S, Bettecken T, Saar K, Linder M, Warnke A, Herpertz-Dahlmann B, Schäfer H, Remschmidt H, Hebebrand J.

J Neural Transm (Vienna). 2007;114(4):513-21. Epub 2006 Nov 10.

PMID:
17093889
5.

[Switching from a short-acting to a long-acting methylphenidate preparation: a multicentre, open study in children with ADHD].

Heger S, Trott GE, Meusers M, Schulz E, Rothenberger A, Rettig K, Medori R, Schreiner A, Remschmidt H; Vertreter der deutschen C-2000-045-Studiengruppe.

Z Kinder Jugendpsychiatr Psychother. 2006 Jul;34(4):257-65. German.

PMID:
16927568
6.

Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in children and adolescents with obsessive-compulsive disorder.

Mössner R, Walitza S, Geller F, Scherag A, Gutknecht L, Jacob C, Bogusch L, Remschmidt H, Simons M, Herpertz-Dahlmann B, Fleischhaker C, Schulz E, Warnke A, Hinney A, Wewetzer C, Lesch KP.

Int J Neuropsychopharmacol. 2006 Aug;9(4):437-42. Epub 2005 Sep 7.

PMID:
16146581
7.

Mutation screen of the brain derived neurotrophic factor gene (BDNF): identification of several genetic variants and association studies in patients with obesity, eating disorders, and attention-deficit/hyperactivity disorder.

Friedel S, Horro FF, Wermter AK, Geller F, Dempfle A, Reichwald K, Smidt J, Brönner G, Konrad K, Herpertz-Dahlmann B, Warnke A, Hemminger U, Linder M, Kiefl H, Goldschmidt HP, Siegfried W, Remschmidt H, Hinney A, Hebebrand J.

Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 5;132B(1):96-9.

PMID:
15457498
8.

Lack of association between the -759C/T polymorphism of the 5-HT2C receptor gene and clozapine-induced weight gain among German schizophrenic individuals.

Theisen FM, Hinney A, Brömel T, Heinzel-Gutenbrunner M, Martin M, Krieg JC, Remschmidt H, Hebebrand J.

Psychiatr Genet. 2004 Sep;14(3):139-42.

PMID:
15318026
9.

No evidence for involvement of alleles of the 825-C/T polymorphism of the G-protein subunit beta 3 in body weight regulation.

Hinney A, Geller F, Neupert T, Sommerlad C, Gerber G, Görg T, Siegfried W, Goldschmidt H, Remschmidt H, Ziegler A, Hebebrand J.

Exp Clin Endocrinol Diabetes. 2001;109(8):402-5.

PMID:
11748488
10.

[Personality disorders and psychiatric comorbidity in obsessive-compulsive disorder and anorexia nervosa].

Müller B, Wewetzer C, Jans T, Holtkamp K, Herpertz SC, Warnke A, Remschmidt H, Herpertz-Dahlmann B.

Fortschr Neurol Psychiatr. 2001 Aug;69(8):379-87. German.

PMID:
11584688
11.

Epidemic obesity: are genetic factors involved via increased rates of assortative mating?

Hebebrand J, Wulftange H, Goerg T, Ziegler A, Hinney A, Barth N, Mayer H, Remschmidt H.

Int J Obes Relat Metab Disord. 2000 Mar;24(3):345-53.

PMID:
10757629
12.

Several mutations in the melanocortin-4 receptor gene including a nonsense and a frameshift mutation associated with dominantly inherited obesity in humans.

Hinney A, Schmidt A, Nottebom K, Heibült O, Becker I, Ziegler A, Gerber G, Sina M, Görg T, Mayer H, Siegfried W, Fichter M, Remschmidt H, Hebebrand J.

J Clin Endocrinol Metab. 1999 Apr;84(4):1483-6.

PMID:
10199800
13.

Systematic mutation screening of the estrogen receptor beta gene in probands of different weight extremes: identification of several genetic variants.

Rosenkranz K, Hinney A, Ziegler A, Hermann H, Fichter M, Mayer H, Siegfried W, Young JK, Remschmidt H, Hebebrand J.

J Clin Endocrinol Metab. 1998 Dec;83(12):4524-7.

PMID:
9851804
14.

Systematic mutation screening of the pro-opiomelanocortin gene: identification of several genetic variants including three different insertions, one nonsense and two missense point mutations in probands of different weight extremes.

Hinney A, Becker I, Heibült O, Nottebom K, Schmidt A, Ziegler A, Mayer H, Siegfried W, Blum WF, Remschmidt H, Hebebrand J.

J Clin Endocrinol Metab. 1998 Oct;83(10):3737-41.

PMID:
9768693

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