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

C J Partsch

Showing results (51-60 of 74) with videos related to

Pageof 8
Sort By:
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|June 29, 2006
Initially elevated TSH and congenital central hypothyroidism due to a homozygous mutation of the TSH beta subunit gene: case report and review of the literatureC-J Partsch, F G Riepe, N Krone, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|April 21, 2007
Endocrine evaluation after endoscopic third ventriculostomy (ETV) in childrenM J Fritsch, M Bauer, C J Partsch, et al.
Pediatric Research|July 10, 1999
Serum leptin levels in patients with progressive central precocious pubertyS Heger, C J Partsch, M Peter, et al.
Hormone Research|January 1, 1997
Growth promotion and Turner-specific bone age after therapy with growth hormone and in combination with oxandrolone: when should therapy be started in Turner syndrome?E E Joss, P E Mullis, E A Werder, et al.
American Journal of Medical Genetics|February 15, 2001
Familial Williams-Beuren syndrome showing varying clinical expressionR Pankau, R Siebert, M Kautza, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|April 26, 2006
Three novel point mutations of the CYP21 gene detected in classical forms of congenital adrenal hyperplasia due to 21-hydroxylase deficiencyN Krone, F G Riepe, C-J Partsch, et al.
European Journal of Endocrinology|September 1, 1994
Variability of pulsatile luteinizing hormone secretion in young male volunteersC J Partsch, S Abrahams, N Herholz, et al.
The Journal of Pediatrics|January 8, 1999
Longitudinal evaluation of growth, puberty, and bone maturation in children with Williams syndromeC J Partsch, G Dreyer, A Gosch, et al.
The Journal of Clinical Endocrinology and Metabolism|September 11, 2001
Longitudinal imaging reveals pituitary enlargement preceding hypoplasia in two brothers with combined pituitary hormone deficiency attributable to PROP1 mutationF G Riepe, C J Partsch, O Blankenstein, et al.
Ceskoslovenska Pediatrie|January 1, 1994
[Growth, development and prediction of body height in children with central precocious puberty after 3 years of therapy with Decapeptyl-Depot, a slow-releasing GnRH agonist]R Hümmelink, W Oostdijk, C J Partsch, et al.
Pageof 8

Showing results (51-60 of 74) with videos related to

Sort By:
Pageof 8
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|June 29, 2006
Initially elevated TSH and congenital central hypothyroidism due to a homozygous mutation of the TSH beta subunit gene: case report and review of the literatureC-J Partsch, F G Riepe, N Krone, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|April 21, 2007
Endocrine evaluation after endoscopic third ventriculostomy (ETV) in childrenM J Fritsch, M Bauer, C J Partsch, et al.
Pediatric Research|July 10, 1999
Serum leptin levels in patients with progressive central precocious pubertyS Heger, C J Partsch, M Peter, et al.
Hormone Research|January 1, 1997
Growth promotion and Turner-specific bone age after therapy with growth hormone and in combination with oxandrolone: when should therapy be started in Turner syndrome?E E Joss, P E Mullis, E A Werder, et al.
American Journal of Medical Genetics|February 15, 2001
Familial Williams-Beuren syndrome showing varying clinical expressionR Pankau, R Siebert, M Kautza, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|April 26, 2006
Three novel point mutations of the CYP21 gene detected in classical forms of congenital adrenal hyperplasia due to 21-hydroxylase deficiencyN Krone, F G Riepe, C-J Partsch, et al.
European Journal of Endocrinology|September 1, 1994
Variability of pulsatile luteinizing hormone secretion in young male volunteersC J Partsch, S Abrahams, N Herholz, et al.
The Journal of Pediatrics|January 8, 1999
Longitudinal evaluation of growth, puberty, and bone maturation in children with Williams syndromeC J Partsch, G Dreyer, A Gosch, et al.
The Journal of Clinical Endocrinology and Metabolism|September 11, 2001
Longitudinal imaging reveals pituitary enlargement preceding hypoplasia in two brothers with combined pituitary hormone deficiency attributable to PROP1 mutationF G Riepe, C J Partsch, O Blankenstein, et al.
Ceskoslovenska Pediatrie|January 1, 1994
[Growth, development and prediction of body height in children with central precocious puberty after 3 years of therapy with Decapeptyl-Depot, a slow-releasing GnRH agonist]R Hümmelink, W Oostdijk, C J Partsch, et al.
Pageof 8