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28篇 您的检索式：作者名="Macchia PE"

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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	High-dose intravenous corticosteroid therapy for Graves' ophthalmopathy显示文摘	Macchia PE Bagattini M Lupoli G	2001	J Endocrinol Invest2001，24，3：	1
3	Increased sensitivity to thyroid hormone in mice with complete deficiency of thyroid hormone receptor alpha 显示文摘	Macchia PE Takeuchi Y Kawai T	2001	Proc Natl Aead Se USA2001，98，1：	1
4	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
5	Recent advances in understanding the molecular basis of primary congenital hypothyroidism显示文摘	Macchia PE	2000	Mol Med Today2000，6，1：	1
6	Recent advances in understanding the molecular basis of primary congenital hypothyroidism显示文摘	Macchia PE	2000	Mol Med Today2000，6，1：	1
7	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
8	Recent advances in understanding the molecular basis of primary congenital hypothyroidism 显示文摘	Macchia PE	2000	Molecular Medicine today2000，6，1：	1
9	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
10	Increased sensitivity to thyroid hormone in mice with complete deficiency of thyroid hormone receptor alpha 显示文摘	Macchia PE Takeuchi Y Kawai T	2001	Proc Natl Acad Sc USA2001，98，1：	1
11	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
12	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
13	Recent advance in understanding the molecular basis of primary congenital hypothyroidism显示文摘	Macchia PE	2002	Mol Med Today2002，6，1：	1
14	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
15	High - dose intravenous corticosteroid therapy for Graves' ophthalmopathy显示文摘	Macchia PE Bagattini M Lupoli G	2001	J Endocrinol Invest2001，24，3：	1
16	Recent advances in understanding the molecular basis of primary congenital hypothyrodism显示文摘	Macchia PE	2000	Mol Med Today2000，6，1：	1
17	Epidermal growth factor receptor in human brain tumors显示文摘	Di-Carlo A Mariano A Macchia PE	1992	J Endocrinol Invest1992，15，1：	1
18	Recent advance in understanding the molecular basis of primary congeniml hypothyroidism显示文摘	Macchia PE	2002	Mol Med Today2002，6，1：	1
19	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
20	Recent advances in understanding the molecular basis of primary congenital hypothyroidism显示文摘	Macchia PE	2000	Mol Med Today2000，6，1：	1

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