H. Grehl

发表

Detection of the CMT1A/HNPP recombination hotspot in unrelated patients of European descent.

J. Lupski, C. van Broeckhoven, J. Martín, 1997, Journal of medical genetics.

Widespread expression of the peripheral myelin protein‐22 gene (pmp22) in neural and non‐neural tissues during murine development

U. Suter, H. Hameister, T. Liehr, 1995, Journal of neuroscience research.

Myotonic dystrophy: Correlation of clinical symptoms with the size of the CTG trinucleotide repeat

D. Claus, R. Fahsold, H. Grehl, 2004, Journal of Neurology.

Atypical Pilocytic Astrocytoma of the Third Ventricle Appearing as a Colloid Cyst

U. Missler, H. Grehl, M. Zimmermann, 2009, Clinical Neuroradiology.

Multifocal motor neuropathy: Clinical and electrophysiological findings

B. Neundörfer, D. Claus, H. Grehl, 1996, Journal of Neurology.

Visualization of the CMT1A duplication and HNPP deletion by FISH on stretched chromosome fibers.

J. Lupski, T. Liehr, B. Rautenstrauss, 1997, Journal of the peripheral nervous system.

PMP22 Thr118Met is not a clinically relevant CMT1 marker

C. van Broeckhoven, B. Rautenstrauss, V. Timmerman, 2000, Journal of Neurology.

Long‐term therapy with high‐dose intravenous immunoglobulins (IVIG) in inflammatory neuropathies

B. Neundörfer, H. Grehl, A. Jaspert, 1997 .

Charcot-Marie-Tooth disease and related peripheral neuropathies: novel mutations in the peripheral myelin genes connexin 32 (Cx32 ), peripheral myelin protein 22 (PMP22 ), and peripheral myelin protein zero (MPZ )

D. Schweitzer, A. Ekici, B. Rautenstrauss, 2000, Neurogenetics.

Estimation of the Mutation Frequencies in Charcot-Marie-Tooth Disease Type 1 and Hereditary Neuropathy with Liability to Pressure Palsies: A European Collaborative Study

X. Estivill, E. Mariman, N. Archidiacono, 1996, European journal of human genetics : EJHG.

Molecular diagnosis of PMP22-associated neuropathies using fluorescence in situ hybridization (FISH) on archival peripheral nerve tissue preparations

T. Liehr, B. Rautenstrauss, H. Grehl, 1997, Acta Neuropathologica.

Clinical and morphological phenotype of HMSN 1A mosaicism

T. Liehr, B. Rautenstrauss, K. Bathke, 1997, Neuromuscular Disorders.

Mosaicism for the Charcot-Marie-Tooth disease type 1A duplication suggests somatic reversion

A. Ekici, T. Liehr, B. Rautenstrauss, 1996, Human Genetics.

Identification of a de novo insertional mutation in P0 in a patient with a Déjérine-Sottas syndrome (DSS) phenotype.

C. van Broeckhoven, B. Rautenstrauss, E. Nelis, 1994, Human molecular genetics.

[Secondary normal pressure hydrocephalus. A complication of chronic neuroborreliosis].

K. Druschky, H. Grehl, H. Stefan, 1999, Der Nervenarzt.

Diagnostic accuracy of plasma glial fibrillary acidic protein for differentiating intracerebral hemorrhage and cerebral ischemia in patients with symptoms of acute stroke.

A. Ferbert, A. Kastrup, G. D. De Marchis, 2012, Clinical chemistry.

Significance of degenerating endoneurial cells in peripheral neuropathy

J. Schröder, H. Grehl, 2004, Acta Neuropathologica.

FISH analysis of interphase nuclei extracted from paraffin-embedded tissue.

T. Liehr, B. Rautenstrauss, H. Grehl, 1995, Trends in genetics : TIG.

Use of FISH analysis for prostate tumors and other tissue types.

T. Liehr, B. Rautenstrauss, H. Grehl, 1997, The American journal of pathology.

A rapid method for FISH analysis on interphase nuclei extracted from cryofixed tissues.

T. Liehr, B. Rautenstrauss, H. Grehl, 1996, Trends in genetics : TIG.

Disposition of clotiazepam: Influence of age, sex, oral contraceptives, cimetidine, isoniazid and ethanol

D. Greenblatt, J. Harmatz, H. Ochs, 2004, European Journal of Clinical Pharmacology.

Histologic evidence for a toxic polyneuropathy due to exposure to 2,3,7,8 — tetrachlorodibenzo‐p‐dioxin (TCDD) in rats

D. Claus, F. Grahmann, H. Grehl, 1993, Acta neurologica Scandinavica.

Accumulation of peripheral myelin protein 22 (PMP22) in onion bulbs of nerves biopsied from patients with different subtypes of Charcot-Marie-Tooth disease type 1

T. Liehr, B. Rautenstrauss, H. Grehl, 1997, Acta Neuropathologica.

Detection oftheCMTlA/HNPPrecombination hotspot inunrelated patients ofEuropean

T. Liehr, B. Rautenstrauss, E. Nelis, 1997 .

Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies: a SacI polymorphism in the proximal CMT1A-REP elements may lead to genetic misdiagnosis

A. Ekici, T. Liehr, B. Rautenstrauss, 1998, Neurogenetics.

[Vasculitic neuropathy in the Garin-Bujadoux-Bannwarth syndrome. A contribution to the understanding of the pathology and pathogenesis of the neurological complications in Lyme borreliosis].

H. Grehl, C. Meier, 2008, Deutsche medizinische Wochenschrift.

Paranoid-halluzinatorische Psychose als Erstmanifestation einer HIV-Infektion

H. Grehl, Kaschka Wp, 1994, Fortschritte der Neurologie-Psychiatrie.

T>C transition in codon 72 (TCG→CCG), S72P, a putative hotspot in PMP22

A. Ekici, B. Rautenstrauss, R. Korinthenberg, 2001, Human mutation.