S Mundlos|J Spranger - JoVE Visualize

Showing results (171-180 of 229) with videos related to

Pageof 23

Sort By:

Clinical Endocrinology|November 5, 2005

Adaptation of the hypothalamic-pituitary hormones during intensive endurance trainingT Bobbert, L Brechtel, K Mai, et al.

Angewandte Chemie (International Ed. in English)|March 7, 2025

Fast Sodium Ion Conductivity in Pristine Na8SnP4: Synthesis, Structure and Properties of the Two Polymorphs LT-Na8SnP4 and HT-Na8SnP4Manuel Botta, Samuel Merk, Robert J Spranger, et al.

American Journal of Human Genetics|June 23, 1998

Acromesomelic dysplasia Maroteaux type maps to human chromosome 9S G Kant, A Polinkovsky, S Mundlos, et al.

International Journal of Obesity (2005)|June 14, 2017

Specific skeletal muscle sphingolipid compounds in energy expenditure regulation and weight gain in Native Americans of Southwestern heritageS Heinitz, P Piaggi, K L Vinales, et al.

American Journal of Medical Genetics|July 1, 1994

Microcephalic osteodysplastic dysplasiaJ H Hersh, M R Joyce, J Spranger, et al.

Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|June 28, 2000

Systemic levels contribute significantly to increased intraocular IGF-I, IGF-II and IGF-BP3 [correction of IFG-BP3] in proliferative diabetic retinopathyJ Spranger, J Bühnen, V Jansen, et al.

Acta Diabetologica|May 29, 2007

Short-term therapy with atorvastatin or fenofibrate does not affect plasma ghrelin, resistin or adiponectin levels in type 2 diabetic patients with mixed hyperlipoproteinaemiaC Otto, B Otto, R J A Frost, et al.

American Journal of Human Genetics|September 14, 2000

Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type BG C Schwabe, S Tinschert, C Buschow, et al.

Deutsche Medizinische Wochenschrift (1946)|April 21, 2005

[Significance of biomarkers for metabolic syndrome during weight reduction]H Rochlitz, S Akpulat, T Bobbert, et al.

American Journal of Medical Genetics|November 7, 1998

Heterozygous glycine substitution in the COL11A2 gene in the original patient with the Weissenbacher-Zweymüller syndrome demonstrates its identity with heterozygous OSMED (nonocular Stickler syndrome)T Pihlajamaa, D J Prockop, J Faber, et al.

Pageof 23

Showing results (171-180 of 229) with videos related to

Sort By:

Pageof 23

Clinical Endocrinology|November 5, 2005

Adaptation of the hypothalamic-pituitary hormones during intensive endurance trainingT Bobbert, L Brechtel, K Mai, et al.

Angewandte Chemie (International Ed. in English)|March 7, 2025

Fast Sodium Ion Conductivity in Pristine Na8SnP4: Synthesis, Structure and Properties of the Two Polymorphs LT-Na8SnP4 and HT-Na8SnP4Manuel Botta, Samuel Merk, Robert J Spranger, et al.

American Journal of Human Genetics|June 23, 1998

Acromesomelic dysplasia Maroteaux type maps to human chromosome 9S G Kant, A Polinkovsky, S Mundlos, et al.

International Journal of Obesity (2005)|June 14, 2017

Specific skeletal muscle sphingolipid compounds in energy expenditure regulation and weight gain in Native Americans of Southwestern heritageS Heinitz, P Piaggi, K L Vinales, et al.

American Journal of Medical Genetics|July 1, 1994

Microcephalic osteodysplastic dysplasiaJ H Hersh, M R Joyce, J Spranger, et al.

Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|June 28, 2000

Systemic levels contribute significantly to increased intraocular IGF-I, IGF-II and IGF-BP3 [correction of IFG-BP3] in proliferative diabetic retinopathyJ Spranger, J Bühnen, V Jansen, et al.

Acta Diabetologica|May 29, 2007

Short-term therapy with atorvastatin or fenofibrate does not affect plasma ghrelin, resistin or adiponectin levels in type 2 diabetic patients with mixed hyperlipoproteinaemiaC Otto, B Otto, R J A Frost, et al.

American Journal of Human Genetics|September 14, 2000

Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type BG C Schwabe, S Tinschert, C Buschow, et al.

Deutsche Medizinische Wochenschrift (1946)|April 21, 2005

[Significance of biomarkers for metabolic syndrome during weight reduction]H Rochlitz, S Akpulat, T Bobbert, et al.

American Journal of Medical Genetics|November 7, 1998

Heterozygous glycine substitution in the COL11A2 gene in the original patient with the Weissenbacher-Zweymüller syndrome demonstrates its identity with heterozygous OSMED (nonocular Stickler syndrome)T Pihlajamaa, D J Prockop, J Faber, et al.

Pageof 23