E-LIB Suche - Ergebnisse für: Heinritz, W.

1

Mutation in Nav1.7 causes high olfactory sensitivity:

Haehner, A. ; Hummel, T. ; Heinritz, W....
European Journal of Pain. 22 (2018) 10 - p. 1767-1773 , 2018

Link: https://doi.org/10.1002/..

2

Evaluation of IP-RP-HPLC for Length Determination of the Tr..:

Skrzypczak, M. ; Heinritz, W. ; Schulz, A. M...
Journal of Chromatographic Science. 48 (2010) 1 - p. 55-58 , 2010

Link: https://doi.org/10.1093/..

3

Multiple trichoepitheliomas – a novel mutation in the CYLD ..:

Amaro, C ; Freitas, I ; Lamarão, P...
Journal of the European Academy of Dermatology and Venereology. 24 (2010) 7 - p. 844-846 , 2010

Link: https://doi.org/10.1111/..

4

CYSTEINE-SPARINGNOTCH3MUTATIONS: CADASIL OR CADASIL VARIANT..:

Scheid, R. ; Heinritz, W. ; Leyhe, T....
Neurology. 71 (2008) 10 - p. 774-776 , 2008

Link: https://doi.org/10.1212/..

5

Evidence for a Founder Effect of the Germline Fumarate Hydr..:

Heinritz, W. ; Paasch, U. ; Sticherling, M....
Annals of Human Genetics. 72 (2008) 1 - p. 35-40 , 2008

Link: https://doi.org/10.1111/..

6

A new mutation in the GJB3 gene in a patient with erythroke..:

Renner, R ; Paasch, U ; Simon, JC..
Journal of the European Academy of Dermatology and Venereology. 22 (2007) 6 - p. 750-751 , 2007

Link: https://doi.org/10.1111/..

7

Vascular parkinsonism in a CADASIL case with an intact nigr..:

Wegner, F. ; Strecker, K. ; Schwarz, J....
Journal of Neurology. 254 (2007) 12 - p. 1743-1745 , 2007

Link: https://doi.org/10.1007/..

8

Vascular parkinsonism and dementia in a CADASIL case with i..:

Wegner, F. ; Strecker, K. ; Schwarz, J....
Aktuelle Neurologie. 33 (2006) S 1 - p. , 2006

Link: https://doi.org/10.1055/..

9

A case of Brooke-Spiegler syndrome with a new mutation in t..:

Heinritz, W. ; Grunewald, S. ; Strenge, S....
British Journal of Dermatology. 154 (2006) 5 - p. 992-994 , 2006

Link: https://doi.org/10.1111/..

10

Hereditäre multiple Exostosen: Molekulargenetische Analyse ..:

Heinritz, W. ; Pretzsch, M. ; Koall, S...
Der Orthopäde. 34 (2005) 5 - p. 470-476 , 2005

Link: https://doi.org/10.1007/..

11

Pre-eclampsia as a 'Three Stage Problem'—A Workshop Report:

Stepan, H ; Faber, R ; Froster, U.G...
Placenta. 25 (2004) 6 - p. 585-587 , 2004

Link: https://doi.org/10.1016/..

12

Another case of autosomal dominant exstrophy of the bladder:

Froster, U. G. ; Heinritz, W. ; Bennek, J...
Prenatal Diagnosis. 24 (2004) 5 - p. 375-377 , 2004

Link: https://doi.org/10.1002/..

13

Detection of five new mutations in the APC gene using denat..:

Heinritz, W ; Kujat, A ; Froster, UG
Clinical Genetics. 63 (2003) 4 - p. 325-327 , 2003

Link: https://doi.org/10.1034/..

14

Molekulargenetischer Mutationsnachweis im PTPN11-Gen beim M..:

Froster, U. G. ; Glander, H.-J. ; Heinritz, W.
Der Hautarzt. 54 (2003) 12 - p. 1190-1192 , 2003

Link: https://doi.org/10.1007/..

15

Erratum:Rare EIF4A2 variants are associated with a neurodev..:

Genetti, CA ; Pinelli, M ; Brunetti-Pierri, N...
https://research.manchester.ac.uk/en/publications/5bb96e6d-bf49-4bef-9208-796742127be1. , 2023

Link: https://research.manches..