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1 . Academic Journal
Genetic interaction of CTLA-4 with HLA-DR15 in multiple sclerosis patients ( Additional members of the Italian Group for MS Genetics and the Portuguese Group for MS Genetics are listed in the Appendix on page 122.).
저자
by
Mehdi Alizadeh
;
Marie-Claude Babron
;
Brigitte Birebent
;
Fumihiko Matsuda
;
Erwann Quelvennec
, et al.
소스
Annals of Neurology; Jul2003, Vol. 54 Issue 1, p119-122, 4p
Full Text (Wiley)
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7 .
Functional SNPs within the Intron 1 of the PROP1 Gene Contribute to Combined Growth Hormone Deficiency (CPHD)
저자
by
Rita Marabese
;
Claudio Bardelli
;
Luigi Tiradani
;
Michela Godi
;
Gianni Bona
, et al.
소스
The Journal of Clinical Endocrinology & Metabolism
. 97:E1791-E1797
Full Text (OUP)
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7 .
Association of HLA class I markers with multiple sclerosis in the Italian and UK population: evidence of two independent protective effects
저자
by
Valeria Bargiggia
;
Patricia Momigliano-Richiardi
;
Maurizio Leone
;
Rosella Mechelli
;
Marco Salvetti
, et al.
소스
Journal of Medical Genetics
. 48:485-492
Full Text (BMJ Journals)
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7 .
HLA-class I markers and multiple sclerosis susceptibility in the Italian population
저자
by
Nadia Barizzone
;
Laura Bergamaschi
;
Daniela Ferrante
;
Roberto Bergamaschi
;
Patricia Momigliano-Richiardi
, et al.
소스
Genes and Immunity
Open Access (OpenAIRE)
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7 .
A novel recessive splicing mutation in the POU1F1 gene causing combined pituitary hormone deficiency
저자
by
G. Corneli
;
Patricia Momigliano-Richiardi
;
Simona Mellone
;
Mara Giordano
;
Yari Carlomagno
, et al.
소스
Journal of Endocrinological Investigation
. 32:653-658
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7 .
Variations in the coding and regulatory sequences of the angiogenin (ANG) gene are not associated to ALS (amyotrophic lateral sclerosis) in the Italian population
저자
by
Patricia Momigliano-Richiardi
;
Laura Bergamaschi
;
Maria Cristina Patrosso
;
Sandra D'Alfonso
;
Fabio Giannini
, et al.
소스
Journal of the Neurological Sciences
. 258:123-127
Full Text (Clinical Key)
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7 .
SOD1 gene mutations in Italian patients with Sporadic Amyotrophic Lateral Sclerosis (ALS)
저자
by
N. Nasuelli
;
Lucia Corrado
;
Maurizio Leone
;
Letizia Mazzini
;
Patricia Momigliano-Richiardi
, et al.
소스
Neuromuscular Disorders
. 16:800-804
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7 .
Concordance, disease progression, and heritability of coeliac disease in Italian twins
저자
by
M.G. Limongelli
;
Luigi Greco
;
Mara Giordano
;
Giuseppe Magazzù
;
Corrado Fagnani
, et al.
소스
Gut
. 55:803-808
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7 .
A variation in a Pit-1 site in the growth hormone gene (GH1) promoter induces a differential transcriptional activity
저자
by
Roberta Paracchini
;
Patricia Momigliano-Richiardi
;
Francesca Giacopelli
;
Michela Godi
;
Simona Mellone
, et al.
소스
Molecular and Cellular Endocrinology
. 249:51-57
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7 .
A Novel Deletion in theGH1Gene Including the IVS3 Branch Site Responsible for Autosomal Dominant Isolated Growth Hormone Deficiency
저자
by
Patricia Momigliano-Richiardi
;
Michela Godi
;
Laura Guazzarotti
;
Daniela Vivenza
;
Berardo di Natale
, et al.
소스
The Journal of Clinical Endocrinology & Metabolism
. 91:980-986
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