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

F Hanefeld

Showing results (61-70 of 197) with videos related to

Pageof 20
Sort By:
Infection|November 1, 1996
Reinfection in Lyme borreliosisH Eiffert, F Hanefeld, R Thomssen, et al.
The British Journal of Dermatology|June 10, 2000
Depigmented hypertrichosis following Blaschko's lines associated with cerebral and ocular malformations: a new neurocutaneous, autosomal lethal gene syndrome from the group of epidermal naevus syndromes?S Schauder, F Hanefeld, U M Noske, et al.
Clinical Dysmorphology|January 29, 2000
Two brothers with Hennekam syndrome and cerebral abnormalitiesP Huppke, H J Christen, B Sattler, et al.
European Journal of Pediatrics|December 1, 1983
Adducted thumb syndrome. Report of a new case and a diagnostic approachJ Kunze, W Park, K H Hansen, et al.
European Journal of Pediatrics|May 1, 1995
Evaluation of the polymerase chain reaction for the detection of Borrelia burgdorferi in cerebrospinal fluid of children with acute peripheral facial palsyH J Christen, H Eiffert, A Ohlenbusch, et al.
Deutsche Medizinische Wochenschrift (1946)|June 7, 1974
[Hypertonic dehydration: a life-threatening condition (author's transl)]H Schachinger, F Hanefeld, H D Frank, et al.
Journal of Inherited Metabolic Disease|July 23, 2003
Striking improvement of muscle strength under creatine therapy in a patient with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyG C Korenke, R J A Wanders, F Hanefeld
Archives of Disease in Childhood|June 27, 2000
Primarily chronic and cerebrovascular course of Lyme neuroborreliosis: case reports and literature reviewM Wilke, H Eiffert, H J Christen, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Normal N-oligosaccharyltransferase activity in fibroblasts from patients with carbohydrate-deficient glycoprotein syndromeR Knauer, L Lehle, F Hanefeld, et al.
Der Nervenarzt|February 1, 1990
[Adrenoleukodystrophy: the significance of peroxisomal disease in adult neurology]R Gold, D H Hunneman, L Kappos, et al.
Pageof 20

Showing results (61-70 of 197) with videos related to

Sort By:
Pageof 20
Infection|November 1, 1996
Reinfection in Lyme borreliosisH Eiffert, F Hanefeld, R Thomssen, et al.
The British Journal of Dermatology|June 10, 2000
Depigmented hypertrichosis following Blaschko's lines associated with cerebral and ocular malformations: a new neurocutaneous, autosomal lethal gene syndrome from the group of epidermal naevus syndromes?S Schauder, F Hanefeld, U M Noske, et al.
Clinical Dysmorphology|January 29, 2000
Two brothers with Hennekam syndrome and cerebral abnormalitiesP Huppke, H J Christen, B Sattler, et al.
European Journal of Pediatrics|December 1, 1983
Adducted thumb syndrome. Report of a new case and a diagnostic approachJ Kunze, W Park, K H Hansen, et al.
European Journal of Pediatrics|May 1, 1995
Evaluation of the polymerase chain reaction for the detection of Borrelia burgdorferi in cerebrospinal fluid of children with acute peripheral facial palsyH J Christen, H Eiffert, A Ohlenbusch, et al.
Deutsche Medizinische Wochenschrift (1946)|June 7, 1974
[Hypertonic dehydration: a life-threatening condition (author's transl)]H Schachinger, F Hanefeld, H D Frank, et al.
Journal of Inherited Metabolic Disease|July 23, 2003
Striking improvement of muscle strength under creatine therapy in a patient with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyG C Korenke, R J A Wanders, F Hanefeld
Archives of Disease in Childhood|June 27, 2000
Primarily chronic and cerebrovascular course of Lyme neuroborreliosis: case reports and literature reviewM Wilke, H Eiffert, H J Christen, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Normal N-oligosaccharyltransferase activity in fibroblasts from patients with carbohydrate-deficient glycoprotein syndromeR Knauer, L Lehle, F Hanefeld, et al.
Der Nervenarzt|February 1, 1990
[Adrenoleukodystrophy: the significance of peroxisomal disease in adult neurology]R Gold, D H Hunneman, L Kappos, et al.
Pageof 20