Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

H Grehl

Showing results (21-30 of 33) with videos related to

Pageof 4
Sort By:
Human Mutation|January 4, 2001
T>C transition in codon 72 (TCG-->CCG), S72P, a putative hotspot in PMP22A B Ekici, O Park, R Korinthenberg, et al.
Human Molecular Genetics|September 1, 1994
Identification of a de novo insertional mutation in P0 in a patient with a Déjérine-Sottas syndrome (DSS) phenotypeB Rautenstrauss, E Nelis, H Grehl, et al.
HNO|November 1, 1992
[Peripheral facial paralysis as the first symptom of unknown metastatic primary tumor]W Schneider, S R Wolf, W D Braunwarth, et al.
Neurogenetics|May 18, 1999
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 misdiagnosisC Fuchs, T Liehr, S Ozbey, et al.
Journal of the Peripheral Nervous System : JPNS|January 1, 1997
Visualization of the CMT1A duplication and HNPP deletion by FISH on stretched chromosome fibersB Rautenstrauss, C Fuchs, T Liehr, et al.
Journal of Neuroscience Research|December 15, 1995
Widespread expression of the peripheral myelin protein-22 gene (PMP22) in neural and non-neural tissues during murine developmentD Baechner, T Liehr, H Hameister, et al.
Neuromuscular Disorders : NMD|January 1, 1997
Clinical and morphological phenotype of HMSN 1A mosaicismH Grehl, B Rautenstrauss, T Liehr, et al.
European Journal of Clinical Pharmacology|January 1, 1984
Disposition of clotiazepam: influence of age, sex, oral contraceptives, cimetidine, isoniazid and ethanolH R Ochs, D J Greenblatt, B Verburg-Ochs, et al.
Human Genetics|July 1, 1996
Mosaicism for the Charcot-Marie-Tooth disease type 1A duplication suggests somatic reversionT Liehr, B Rautenstrauss, H Grehl, et al.
Clinical Neuropathology|August 12, 1999
Neuropeptide content of peripheral nerve in relation to nerve function in neuropathyA Bickel, H Grehl, M Butz, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Human Mutation|January 4, 2001
T>C transition in codon 72 (TCG-->CCG), S72P, a putative hotspot in PMP22A B Ekici, O Park, R Korinthenberg, et al.
Human Molecular Genetics|September 1, 1994
Identification of a de novo insertional mutation in P0 in a patient with a Déjérine-Sottas syndrome (DSS) phenotypeB Rautenstrauss, E Nelis, H Grehl, et al.
HNO|November 1, 1992
[Peripheral facial paralysis as the first symptom of unknown metastatic primary tumor]W Schneider, S R Wolf, W D Braunwarth, et al.
Neurogenetics|May 18, 1999
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 misdiagnosisC Fuchs, T Liehr, S Ozbey, et al.
Journal of the Peripheral Nervous System : JPNS|January 1, 1997
Visualization of the CMT1A duplication and HNPP deletion by FISH on stretched chromosome fibersB Rautenstrauss, C Fuchs, T Liehr, et al.
Journal of Neuroscience Research|December 15, 1995
Widespread expression of the peripheral myelin protein-22 gene (PMP22) in neural and non-neural tissues during murine developmentD Baechner, T Liehr, H Hameister, et al.
Neuromuscular Disorders : NMD|January 1, 1997
Clinical and morphological phenotype of HMSN 1A mosaicismH Grehl, B Rautenstrauss, T Liehr, et al.
European Journal of Clinical Pharmacology|January 1, 1984
Disposition of clotiazepam: influence of age, sex, oral contraceptives, cimetidine, isoniazid and ethanolH R Ochs, D J Greenblatt, B Verburg-Ochs, et al.
Human Genetics|July 1, 1996
Mosaicism for the Charcot-Marie-Tooth disease type 1A duplication suggests somatic reversionT Liehr, B Rautenstrauss, H Grehl, et al.
Clinical Neuropathology|August 12, 1999
Neuropeptide content of peripheral nerve in relation to nerve function in neuropathyA Bickel, H Grehl, M Butz, et al.
Pageof 4