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M Bettendorf

Showing results (31-40 of 48) with videos related to

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Human Molecular Genetics|December 1, 1996
Identification of non-amplifying CYP21 genes when using PCR-based diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH) affected pedigreesD J Day, P W Speiser, E Schulze, et al.
Cell Death & Disease|January 11, 2024
Low androgen signaling rescues genome integrity with innate immune response by reducing fertility in humansJ Zimmer, L Mueller, P Frank-Herrmann, et al.
European Journal of Pediatrics|April 17, 1999
Lymphocytic hypophysitis with central diabetes insipidus and consequent panhypopituitarism preceding a multifocal, intracranial germinoma in a prepubertal girlM Bettendorf, M Fehn, J Grulich-Henn, et al.
Endocrine Research|February 1, 1995
Divergence between genotype and phenotype in relatives of patients with the intron 2 mutation of steroid-21-hydroxylaseE Schulze, G Scharer, A Rogatzki, et al.
The Journal of Infectious Diseases|January 1, 2003
Prognostic value of baseline human immunodeficiency virus type 1 DNA measurement for disease progression in patients receiving nucleoside therapyCamlin Tierney, Janet L Lathey, Cindy Christopherson, et al.
Journal of the American Dental Association (1939)|September 3, 2010
Treating dentin hypersensitivity: therapeutic choices made by dentists of the northwest PRECEDENT networkJoana Cunha-Cruz, John C Wataha, Lingmei Zhou, et al.
Hormone Research|August 20, 2009
Is the response to growth hormone in short children born small for gestational age dependent on genetic or maternal factors?Otto Mehls, A Lindberg, M Bettendorf, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 1, 2000
Diagnosis and management of juvenile hyperthyroidism in Germany: a retrospective multicenter studyJ Dötsch, T Siebler, B P Hauffa, et al.
Human Molecular Genetics|February 1, 1994
Congenital adrenal hyperplasia caused by a novel homozygous frameshift mutation 273 delta AA in type II 3 beta-hydroxysteroid dehydrogenase gene (HSD3B2) in three male patients of Afghan/Pakistani originJ Simard, E Rhéaume, J F Leblanc, et al.
Klinische Padiatrie|August 31, 2001
Obesity after childhood craniopharyngioma--German multicenter study on pre-operative risk factors and quality of lifeH L Müller, K Bueb, U Bartels, et al.
Pageof 5

Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
Human Molecular Genetics|December 1, 1996
Identification of non-amplifying CYP21 genes when using PCR-based diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH) affected pedigreesD J Day, P W Speiser, E Schulze, et al.
Cell Death & Disease|January 11, 2024
Low androgen signaling rescues genome integrity with innate immune response by reducing fertility in humansJ Zimmer, L Mueller, P Frank-Herrmann, et al.
European Journal of Pediatrics|April 17, 1999
Lymphocytic hypophysitis with central diabetes insipidus and consequent panhypopituitarism preceding a multifocal, intracranial germinoma in a prepubertal girlM Bettendorf, M Fehn, J Grulich-Henn, et al.
Endocrine Research|February 1, 1995
Divergence between genotype and phenotype in relatives of patients with the intron 2 mutation of steroid-21-hydroxylaseE Schulze, G Scharer, A Rogatzki, et al.
The Journal of Infectious Diseases|January 1, 2003
Prognostic value of baseline human immunodeficiency virus type 1 DNA measurement for disease progression in patients receiving nucleoside therapyCamlin Tierney, Janet L Lathey, Cindy Christopherson, et al.
Journal of the American Dental Association (1939)|September 3, 2010
Treating dentin hypersensitivity: therapeutic choices made by dentists of the northwest PRECEDENT networkJoana Cunha-Cruz, John C Wataha, Lingmei Zhou, et al.
Hormone Research|August 20, 2009
Is the response to growth hormone in short children born small for gestational age dependent on genetic or maternal factors?Otto Mehls, A Lindberg, M Bettendorf, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 1, 2000
Diagnosis and management of juvenile hyperthyroidism in Germany: a retrospective multicenter studyJ Dötsch, T Siebler, B P Hauffa, et al.
Human Molecular Genetics|February 1, 1994
Congenital adrenal hyperplasia caused by a novel homozygous frameshift mutation 273 delta AA in type II 3 beta-hydroxysteroid dehydrogenase gene (HSD3B2) in three male patients of Afghan/Pakistani originJ Simard, E Rhéaume, J F Leblanc, et al.
Klinische Padiatrie|August 31, 2001
Obesity after childhood craniopharyngioma--German multicenter study on pre-operative risk factors and quality of lifeH L Müller, K Bueb, U Bartels, et al.
Pageof 5