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19篇 您的检索式：作者名="Pfarr N"

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		题名	作者	年代	出处	被引量
	1	Hemodynamic and clinical onset in patients with hereditary pulmonary arterial hypertension and BMPR2 mutations显示文摘	Pfarr N Szamalek-Hoegel J Fischer C	2011	Respir Res2011，12，1：	1
	2	Subclinical hyperthy- roidism due to a thyrotropin receptor (TSHR) gene mutation (S505R)显示文摘	Pohlenz J Pfarr N Kruger S	2006	ActaPaediatr2006，95，12：	1
	3	Congenital hypothyroidism caused by new mutations in the thyroid oxidase 2(THOX2)gene显示文摘	Pfarr N Korsch E Kaspers S	2006	Clin Endocrinol(Oxf)2006，65，6：	1
	4	Congenital hypothyroidism caused by new mutations in the thyroid oxidase 2 (THOX2) gene显示文摘	Pfarr N Korsch E Kaspers S	2006	Clin Endocrinol2006，65，6：	1
	5	Mild congenital primary hypothyroidism in a Turkish family caused by a homozygous missense thyrotropin receptor (TSHR) gene mutation(A593V)显示文摘	Fricke-Otto S Pfarr N Muhlenberg R	2005	Exp Clin Endocrinol Diabetes2005，113，10：	1
	6	Hemodynamic and genetic analysis in children with idiopathic, heritable, and congenital heart dis- ease associated pulmonary arterial hypertension显示文摘	Pfarr N Fischer C Ehlken N	2013	Respir Res2013，14，1：	1
	7	Congenital primary hypothyroidism in a turkish family caused by a homozygons nonsense mutation(R609X)in the thyrotropin receptor gene显示文摘	Richter-Unruh A Hauffa BP Pfarr N	2004	Thyroid2004，14，11：	1
	8	Congenital hypothyroidism caused by new mutations in the thyroid oxidase 2 (THOX2) gene 显示文摘	Pfarr N Korsch E Kaspers S	2006	Clin Endocrinol (Oxf)2006，65，：	1
	9	Congenital hypothyroidism caused by new mutations in the thyroid oxidase 2(THOX2)gene显示文摘	Pfarr N Korsch E Kaspers S	2006	Clin Endocrinol(Oxf)2006，65，6：	1
	10	Hemodynamic and genetic analysis in children with idiopathic, heritable, and congenital heart disease associated pulmonary arterial hypertension 显示文摘	Pfarr N Fischer C Ehlken N	2013	Respir Res2013，14，：	1
	11	Congenital hypothyroidism caused by new mutations in the thyroid oxidase 2 ( THOX2 ) gene 显示文摘	Pfarr N Korsch E Kaspers S	2006	Clin Endocrinol ( Oxf)2006，65，6：	1
	12	Congenital primary hypothyroidism in a turkish family: caused by a homozygous nonsense mutation (R609X) in the thyrotropin receptor gene 显示文摘	Richter-Unruh A Hauffa BP Pfarr N	2004	Thyroid2004，14，：	1
	13	Congenital hypothyroidism caused by new mutations in the thyroid oxidase 2 ( THOX2 ) gene 显示文摘	Pfarr N Korsch E Kaspers S	2006	Clin Endocrinol (Oxf)2006，65，6：	1
	14	Mild congenital primary hypothyroidism in a Turkish family caused by a homozygous missense thyrotropin receptor (TSHR) gene mutation ( A593 V ) 显示文摘	Fricke - Otto S Pfarr N Muhlenberg R	2005	Exp Clin Endocrinol Diabetes2005，113，10：	1
	15	Congenital primary hypothyroidism in a turkish family caused by a homozygous nonsense mutation (R609X) in the thyrotropin receptor gene显示文摘	Richter U A Hauffa B P Pfarr N	2004	Thyroid2004，14，11：	1
	16	Mutations in POLE and survival of colorectal cancer patients-link to disease stage and treatment显示文摘	Stenzinger A Pfarr N Endris V et aJ	2014	Cancer Med2014，3，6：	1
	17	Congenital hypothyroidism caused by new mutations in the thyroid oxidase 2 (THOX2) gene显示文摘	Pfarr N Korsch E Kaspers S	2006	Clin Endocrinol (Oxf)2006，65，6：	1
	18	Mild congenital primary hypothyroidism in a Turkish family caused by a homozygous missense thyrotropin receptor (TSHR) gene mutation (A593 V)显示文摘	Fricke-Otto S Pfarr N Muhlenberg R	2005	Exp Clin Endocrinol Diabetes2005，113，10：	1
	19	Hemodynamic and clini- cal onset in patients with hereditary pulmonary arterial hypertension and BMPR2 mutations显示文摘	Pfarr N Szamalek - Hoegel J Fischer C	2011	Respir Res2011，12，：	1

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