OÄ Dr. med. Ulrike Grieben

Oberärztin

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Telefon: +49 30 450 540507 (Hochschulambulanz)
Fax:      +49 30 450 540907






Projekte und Verantwortungsbereich


Oberärztin der Hochschulambulanz für Muskelkrankheiten
Does Vitamin D deficiency support myalgia?                              
A clinical outcome study for dysferlinopathy


Scientfic background

1974-1978         
Medical Study (Goettingen)

1976-1979         
Doctoral Thesis (Max-Planck-lnstitute for Biophysical Chemistry, Goettingen, Prof. Dr. Otto Creutzfeldt)

1978-1979         
Internal Year (ZKH Hospital Bremen-Mitte)

1979-1983         
Assistant Doctor (Prof.-Hess, Children`s hospital ZKH Bremen-Mitte)

1983-1984         
Assistant Doctor (Municipal Hospital Offenbach)

1984-1986         
Senior Physician (Children`s Hospital - Municipal Hospital Offenbach)

1986-1996         
Senior Physician (Children`s Hospital University of Mainz)

1996-2010         
Senior Physician (Center for Social Pediatrics Charité - specialised on neuromuscular diseases and myelodysplasia)

2000                 
Additional Qualification Grief Counseling

2009                 
Examination: Additional Title Neuropediatrician


Publications

4 multi-centric clinical studies 1993, 1094, 2004, 2007.
Valadares ER, Pizarro MX, Oliveira LR, Amorim RH, Pinheiro TM, Grieben U, Santos HH, Queiroz RR, Lopes Gde C, Godard AL. Juvenile neuronal ceroid-lipofuscinosis: clinical and molecular investigation in a !arge family in Brazil. Arq Neuropsiquiatr.  2011 Feb;69(1):13-8

Kirschner J, Schessl J, Schara U, Reitter B, Stettner GM, Hobbiebrunken E, Wilichowski E, Bernert G, Weiss S, Stehling F, Wiegand G, Müller-Felber W, Thiele S, Grieben U, von der Hagen M, Lütschg J, Schmoor C, lhorst G, Korinthenberg  R. Treatment  of Duchenne muscular dystrophy with ciclosporin  A: a randomised, double-blind, placebo-controlled multicentre trial. Lancet NeuroI. 2010 Nov;9(11):1053-9

Klopocki E, Graui-Neumann LM, Grieben U, Tönnies H, Ropers HH, Horn D, Mundlos S, Ullmann R. A Further case of the recurrent 15q24 microdeletion  syndrome, detected by array CGH. Eur J Pediatr. 2008 Aug;167(8):903-8

von der Hagen M, Schallner J, Kaindl AM, Koehler K, Mitzscherling P, Abicht A, Grieben U, Korinthenberg R, Kress W, von Moers A, Müller JS, Schara U, Vorgerd M, Walter MC, Müller-Reible  C, Hübner C, Lochmüller  H, Huebner A. Facing the genetic heterogeneity in neuromuscular disorders: linkage analysis as an economic diagnostic approach towards the molecular diagnosis.  Neuromuscul Disord. 2006 Jan;16(1):4-13

Thiel C, Schwarz M, Hasilik M, Grieben U, Hanefeld F, Lehle L, von Figura K, Körner C. Deficiency  of dolichyi-P-Man: Man7GicNAc2-PP-dolichyl mannosyltransferase causes congenital disorder of glycosylation type lg. Biochem J. 2002 Oct 1;367(Pt 1):195-201.

Pfeifle J, Grieben U, Bork K. [Bromoderma tuberosum caused by anticonvulsive  treatment with potassium bromide]. Hautarzt. 1992 Dec; 43(12):792-4.  German