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 (81-90 of 197) with videos related to

Pageof 20
Sort By:
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|March 1, 1982
[Long-term sequelae of neonatal group B streptococcal septicemia/meningitis (author's transl)]H Schröder, J Tessmar, H Paust, et al.
Neuropediatrics|June 1, 2000
Congenital disorder of glycosylation-Ic: case report and genetic defectF Hanefeld, C Körner, U Holzbach-Eberle, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|October 29, 2000
Aminophylline modulation of the mouse respiratory network changes during postnatal maturationB Wilken, J M Ramirez, F Hanefeld, et al.
Lancet (London, England)|December 5, 1987
Treatment with ursodeoxycholic acid renders children with biliary atresia suitable for liver transplantationD Ullrich, D Rating, W Schröter, et al.
Journal of Child Neurology|August 1, 1997
Intrathecal IgA synthesis in X-linked cerebral adrenoleukodystrophyG C Korenke, H Reiber, D H Hunneman, et al.
European Journal of Endocrinology|February 14, 1998
Hyperphagia in children with craniopharyngioma is associated with hyperleptinaemia and a failure in the downregulation of appetiteC Roth, B Wilken, F Hanefeld, et al.
Archives of Disease in Childhood|July 1, 1973
Congenital adrenal hyperplasia. Report of a case with neurological complicationsF Hanefeld, L Crome, N E France, et al.
Human Genetics|January 1, 1987
Genetic linkage study between the loci for Duchenne and Becker muscular dystrophy and nine X-chromosomal DNA markersE Wilichowski, M Krawczak, E Seemanova, et al.
Brain & Development|January 1, 1985
Rett syndrome: criteria for inclusion and exclusionB Hagberg, F Goutières, F Hanefeld, et al.
Neuropediatrics|June 21, 2002
Altered methylation pattern of the G6 PD promoter in Rett syndromeP Huppke, S Bohlander, N Krämer, et al.
Pageof 20

Showing results (81-90 of 197) with videos related to

Sort By:
Pageof 20
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|March 1, 1982
[Long-term sequelae of neonatal group B streptococcal septicemia/meningitis (author's transl)]H Schröder, J Tessmar, H Paust, et al.
Neuropediatrics|June 1, 2000
Congenital disorder of glycosylation-Ic: case report and genetic defectF Hanefeld, C Körner, U Holzbach-Eberle, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|October 29, 2000
Aminophylline modulation of the mouse respiratory network changes during postnatal maturationB Wilken, J M Ramirez, F Hanefeld, et al.
Lancet (London, England)|December 5, 1987
Treatment with ursodeoxycholic acid renders children with biliary atresia suitable for liver transplantationD Ullrich, D Rating, W Schröter, et al.
Journal of Child Neurology|August 1, 1997
Intrathecal IgA synthesis in X-linked cerebral adrenoleukodystrophyG C Korenke, H Reiber, D H Hunneman, et al.
European Journal of Endocrinology|February 14, 1998
Hyperphagia in children with craniopharyngioma is associated with hyperleptinaemia and a failure in the downregulation of appetiteC Roth, B Wilken, F Hanefeld, et al.
Archives of Disease in Childhood|July 1, 1973
Congenital adrenal hyperplasia. Report of a case with neurological complicationsF Hanefeld, L Crome, N E France, et al.
Human Genetics|January 1, 1987
Genetic linkage study between the loci for Duchenne and Becker muscular dystrophy and nine X-chromosomal DNA markersE Wilichowski, M Krawczak, E Seemanova, et al.
Brain & Development|January 1, 1985
Rett syndrome: criteria for inclusion and exclusionB Hagberg, F Goutières, F Hanefeld, et al.
Neuropediatrics|June 21, 2002
Altered methylation pattern of the G6 PD promoter in Rett syndromeP Huppke, S Bohlander, N Krämer, et al.
Pageof 20