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Author/Creator Garin, Intza

1. From pseudohypoparathyroidism to inactivating PTH/PTHrP signalling disorder (iPPSD), a novel classification proposed by the EuroPHP network. Issue 6 (December 2016)

Authors:
Thiele, Susanne; Mantovani, Giovanna; Barlier, Anne; Boldrin, Valentina; Bordogna, Paolo; De Sanctis, Luisa; Elli, Francesca M; Freson, Kathleen; Garin, Intza; Grybek, Virginie; Hanna, Patrick; Izzi, Benedetta; Hiort, Olaf; Lecumberri, Beatriz; Pereda, Arrate; Saraff, Vrinda; Silve, Caroline; Tur...
Journal:
European journal of endocrinology
Issue:
Volume 175:Issue 6(2016)
Page Start:
P1
Record Type:
Journal Article
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2. Genome-wide DNA methylation analysis of pseudohypoparathyroidism patients with GNAS imprinting defects. Issue 1 (December 2016)

Authors:
Rochtus, Anne; Martin-Trujillo, Alejandro; Izzi, Benedetta; Elli, Francesca; Garin, Intza; Linglart, Agnes; Mantovani, Giovanna; Perez de Nanclares, Guiomar; Thiele, Suzanne; Decallonne, Brigitte; Van Geet, Chris; Monk, David; Freson, Kathleen
Journal:
Clinical epigenetics
Issue:
Volume 8:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
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3. Genome‐Wide Allelic Methylation Analysis Reveals Disease‐Specific Susceptibility to Multiple Methylation Defects in Imprinting Syndromes. Issue 4 (19th February 2013)

Authors:
Court, Franck; Martin‐Trujillo, Alex; Romanelli, Valeria; Garin, Intza; Iglesias‐Platas, Isabel; Salafsky, Ira; Guitart, Miriam; Perez de Nanclares, Guiomar; Lapunzina, Pablo; Monk, David
Journal:
Human mutation
Issue:
Volume 34:Issue 4(2013:Apr.)
Page Start:
595
Record Type:
Journal Article
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