Stoeber G - Search Results

1

Improvement of prefrontal brain function in endogenous psychoses under atypical antipsychotic treatment.

Ehlis AC, Herrmann MJ, Pauli P, Stoeber G, Pfuhlmann B, Fallgatter AJ. Ehlis AC, et al. Among authors: stoeber g. Neuropsychopharmacology. 2007 Aug;32(8):1669-77. doi: 10.1038/sj.npp.1301293. Epub 2007 Jan 3. Neuropsychopharmacology. 2007. PMID: 17203015 Clinical Trial.

2

Postpartum psychoses: prognosis, risk factors, and treatment.

Pfuhlmann B, Stoeber G, Beckmann H. Pfuhlmann B, et al. Among authors: stoeber g. Curr Psychiatry Rep. 2002 Jun;4(3):185-90. doi: 10.1007/s11920-002-0025-6. Curr Psychiatry Rep. 2002. PMID: 12003680 Review.

3

Sensory gating deficit in a subtype of chronic schizophrenic patients.

Ringel TM, Heidrich A, Jacob CP, Pfuhlmann B, Stoeber G, Fallgatter AJ. Ringel TM, et al. Among authors: stoeber g. Psychiatry Res. 2004 Mar 15;125(3):237-45. doi: 10.1016/j.psychres.2004.01.004. Psychiatry Res. 2004. PMID: 15051184

4

Specific P300 features in patients with cycloid psychosis.

Strik WK, Fallgatter AJ, Stoeber G, Franzek E, Beckmann H. Strik WK, et al. Among authors: stoeber g. Acta Psychiatr Scand. 1996 Dec;94(6):471-6. doi: 10.1111/j.1600-0447.1996.tb09893.x. Acta Psychiatr Scand. 1996. PMID: 9021002

5

Specific P300 features in patients with cycloid psychosis.

Strik WK, Fallgatter AJ, Stoeber G, Franzek E, Beckmann H. Strik WK, et al. Among authors: stoeber g. Acta Psychiatr Scand. 1997 Jan;95(1):67-72. doi: 10.1111/j.1600-0447.1997.tb00376.x. Acta Psychiatr Scand. 1997. PMID: 9051164

6

Is FKBP5 a genetic marker of affective psychosis? A case control study and analysis of disease related traits.

Gawlik M, Moller-Ehrlich K, Mende M, Jovnerovski M, Jung S, Jabs B, Knapp M, Stoeber G. Gawlik M, et al. Among authors: stoeber g. BMC Psychiatry. 2006 Nov 2;6:52. doi: 10.1186/1471-244X-6-52. BMC Psychiatry. 2006. PMID: 17081296 Free PMC article.

7

Analysis of GABRB2 association with schizophrenia in German population with DNA sequencing and one-label extension method for SNP genotyping.

Yu Z, Chen J, Shi H, Stoeber G, Tsang SY, Xue H. Yu Z, et al. Among authors: stoeber g. Clin Biochem. 2006 Mar;39(3):210-8. doi: 10.1016/j.clinbiochem.2006.01.009. Epub 2006 Feb 9. Clin Biochem. 2006. PMID: 16472798

8

Fetal open spinal dysraphism repair through a mini-hysterotomy: Influence of gestational age at surgery on the perinatal outcomes and postnatal shunt rates.

Peralta CFA, Botelho RD, Romano ER, Imada V, Lamis F, Júnior RR, Nani F, Stoeber GH, de Salles AAF. Peralta CFA, et al. Among authors: stoeber gh. Prenat Diagn. 2020 May;40(6):689-697. doi: 10.1002/pd.5675. Epub 2020 Mar 9. Prenat Diagn. 2020. PMID: 32112579

9

Father-to-son transmission of an X-linked gene: a case of paternal sex chromosome heterodisomy.

Ferrier RA, Lowry RB, Lemire EG, Stoeber GP, Howard J, Parboosingh JS. Ferrier RA, et al. Among authors: stoeber gp. Am J Med Genet A. 2009 Dec;149A(12):2871-3. doi: 10.1002/ajmg.a.32994. Am J Med Genet A. 2009. PMID: 19921643 No abstract available.

10

Novel mutations and polymorphisms in genes causing hereditary hemorrhagic telangiectasia.

Abdalla SA, Cymerman U, Rushlow D, Chen N, Stoeber GP, Lemire EG, Letarte M. Abdalla SA, et al. Among authors: stoeber gp. Hum Mutat. 2005 Mar;25(3):320-1. doi: 10.1002/humu.9312. Hum Mutat. 2005. PMID: 15712271

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