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28篇 您的检索式：作者名="Biebermann"

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	题名	作者	年代	出处	被引量
1	Neonatal thyroid disorders 显示文摘	Gruters A Biebermann H Krude H	2003	Horm Res2003，，591：	1
2	Molecular genetic defects in congenital hypothyroidism显示文摘	Gruters A Krude H Biebermann H	2004	Eur J Endocrinol2004，151，3：	1
3	Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation显示文摘	Friesema EC Grueters A Biebermann H	2004	Lancet2004，364，：	1
4	Proinsulin and the proinsulin/insulin ratio in overweight and obese children and adoles- cents:Relation to clinical parameters, insulin resistance, and impaired glucose regulation 显示文摘	Von Berghes C Brabant G Biebermann H	2011	Pediatr Diabetes2011，12，32：	1
5	Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans显示文摘	Biebermann H Luck W	1998	Nature Genet1998，19，：	1
6	Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation 显示文摘	Friesema EC Grueters A Biebermann H	2004	Lancet2004，364，9443：	1
7	Congenital hyperthyroidism显示文摘	KRUDE H BIEBERMANN H KROHN HP	1997	Exp Clin Endocfinol Diabetes1997，105，4：	1
8	Obesity due to proopiomelanocortin deficien-cy: three new cases and treatment trials with thyroid hormone and ACTH4-10 显示文摘	Krude H Biebermann H Schnabel D	2003	J Clin Endocrinol Metab2003，88，：	1
9	Mutations of the human thyrotropin receptor gene causing thyroid hypoplasia and persistent congenital hypothyroidism显示文摘	Biebermann H Schoneberg T Krude H	1997	J Clin Endocrinol Metab1997，82，10：	1
10	Severe early-onset obesity,adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans 显示文摘	Krude H Biebermann H	1998	Nat Genet1998，19，：	1
11	Mutations of the human thyrotropin receptor gene causing thyroid hypoplasia and persistent congenital hypothyroidism 显示文摘	Biebermann H Schoneberg T Krude H	1997	J Clin Endocrinol Metab1997，82，10：	1
12	Mutant G-proteincoupled receptors as a cause of human disease显示文摘	Schoneberg T Schulz A Biebermann H	2004	Pharmacol Ther2004，104，：	1
13	Severe early-onset obesity,adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans显示文摘	Krude H Biebermann H Luck W		0，，02：	1
14	Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans显示文摘	Krude H Biebermann H Luck W	1998	Nat Genet1998，19，：	1
15	Mutant G- protein-coupled receptors as a cause of human diseases 显示文摘	Schoneberg T Schulz A Biebermann H	2004	Pharmacol Ther2004，104，3：	1
16	Association between mutations in a thyroid hormone transporter and severe X- linked psychomotor retardation 显示文摘	Friesema EC Grueters A Biebermann H	2004	Lancet2004，364，14：	1
17	Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in human显示文摘	Biebermann H Luck W Horn R Brabant G Gruters A	1998	Nat Genet1998，19，：	1
18	Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency显示文摘	Krude H Schtz B Biebermann H	2002	J Clin Invest2002，109，4：	1
19	Congenital hyperthyroidism显示文摘	KRUDE H BIEBERMANN H KROHN H P	1997	Exp Clin Endocrinol Diabetes1997，105，4：	1
20	Autosomal-dominant mode of inheritance of a melan-ocortin-4 receptor mutation in a patient with severe early-onset obesity is due to a domin antnegative effect caused by receptor dimerization显示文摘	BIEBERMANN H KRUDE H ELSNER A	2003	Diabetes2003，52，：	1

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