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24篇 您的检索式：作者名="LAPI P"

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	题名	作者	年代	出处	被引量
1	PAX8 mutations asso- ciated with congenital hypothyroidism caused by thyroid dysgenesis 显示文摘	Macchia PE Lapi P Krude H etal	1998	Nat Genet1998，19，1：	1
2	The fate of Schwann cells transplanted in the brain during development显示文摘	Baron-Van Evercooren A Clerin-Duhamel E Lapie P	1992	Dev Neurosci1992，14，2：	1
3	Cloning,chromosomal localization and identification of polymorphisms in the human thyroid transcription factor 2 gene(TITF2) 显示文摘	Mattei MG Lapi P	1999	Biochimie1999，81，4：	1
4	Geometric characteristics of arterial network of rat pial microcirculation显示文摘	LAPI D MARCHIAFAVA P L COLANTUONI A	2008	Vasc Res2008，45，：	1
5	Absence of HTLV-1 DNA se- quences in cutaneous T-cell lymphoma/mycosis fungoides 显示文摘	Lapis P Freeman J Bitter MA	1992	Acta- Morphologica Hungarica1992，40，14：	1
6	PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis 显示文摘	Macchia PE Lapi P Krude H	1998	Nat Genet1998，19，1：	1
7	Mutations in the gene for thyroid transcription factor-Ⅰ(TTF-Ⅰ) are not a frequent cause of congenital hypothyroidism (CH) with thyroud dysgenesis 显示文摘	Lapi P Macchia PE Chiovatoo L	1997	Thyroid1997，7，3：	1
8	Cloning, chro- mosomal localization and identification of polymorphisms in the human thyroid transcription factor 2 gene (TITF2) 显示文摘	Macchia PE Mattei MG Lapi P	1999	Biochimie1999，81，5：	1
9	Cloning, chromosomal localization and identification of polymorphisms in the human thyroid transcription factor 2 gene(TITF2)显示文摘	MACCHIA P E MATTEI M G LAPI P	1999	Biochimie1999，81，5：	1
10	PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis显示文摘	Macchia PE Lapi P Krude H	1998	Nat Genet1998，19，1：	1
11	PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis 显示文摘	Macchia PE Lapi P Krude H	1998	Nat Genet1998，19，：	1
12	Cloning,chromosomal localization and identification of polymorphisms in the human thyroid transcription factor 2 gene{TTTF2}显示文摘	Mattei MG Lapi P	1999	Biochimie1999，81，4：	1
13	Cloning, chromosomal localization and identification of palymorphisms in the human thyroid transcription factor 2 gene (TITF-2)显示文摘	Maechia PE Mattei MG Lapi P	1999	Biochimie1999，81，5：	1
14	Effects of heavy metal pollution on soil macrofauna in a grassland of Northern France显示文摘	Nahmani J Lavelle P Lapied E	2002	European Journal of Soil Biology2002，38，34：	1
15	En- zyme - mediated epoxidation of methyl oleate supported by imidazolium- based ionic liquids 显示文摘	SILVA W S D LAPIS A A M SUAREZ P A Z	2011	J Mol Catal B Enzym2011，68，1：	1
16	Hypokalemic periodic paralysis: an autosomal dominant muscle disorder caused by mutations in a voltage-gated calcium channel显示文摘	Lapie P Lory P Fontaine B	1997	Neuromuscul Disord1997，7，4：	1
17	PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis显示文摘	MACCHIA P E LAPI P KRUDE H	1998	Nature Genetics1998，19，1：	1
18	Effects of heavy metal soil pollution on earthworm communities in the north of France显示文摘	Nahmani J Lavelle P Lapied E van Oort F	2003	Pedobiologia2003，47，5：	1
19	Immunohictcohemical detection of PGDF in fibrotic liver disease显示文摘	Schaff Z Lapis K	1998	Hepatology1998，28，4：	1
20	Cloning, chromoso- mal localization and identification of polymorphisms in the human thyroid transcription factor 2 gene (TITF2)显示文摘	Macchia PE Mattei MG Lapi P	1999	Bin- chimie1999，81，5：	1

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