Publications by authors named "Tiina Robins"

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Progranulin mutation causes frontotemporal dementia in the Swedish Karolinska family.
Huei-Hsin Chiang, Lina Rosvall, Jesper Brohede, Karin Axelman, Behnosh F Björk, Tiina Robins

Alzheimers Dement· November 2008

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Three novel CYP21A2 mutations and their protein modelling in patients with classical 21-hydroxylase deficiency from northeastern Iran.
Alireza Baradaran-Heravi, Rahim Vakili, Tiina Robins, Jonas Carlsson, Nosrat Ghaemi

Clin Endocrinol (Oxf)· September 2007

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Characterization of novel missense mutations in CYP21 causing congenital adrenal hyperplasia.
Tiina Robins, Christine Bellanne-Chantelot, Michela Barbaro, Sylvie Cabrol, Anna Wedell

J Mol Med (Berl)· March 2007

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Molecular model of human CYP21 based on mammalian CYP2C5: structural features correlate with clinical severity of mutations causing congenital adrenal hyperplasia.
Tiina Robins, Jonas Carlsson, Maria Sunnerhagen, Anna Wedell, Bengt Persson

Mol Endocrinol· November 2006

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Not all amino acid substitutions of the common cluster E6 mutation in CYP21 cause congenital adrenal hyperplasia.
Tiina Robins, Michela Barbaro, Svetlana Lajic, Anna Wedell

J Clin Endocrinol Metab· April 2005

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Novel mutations in CYP21 detected in individuals with hyperandrogenism.
Svetlana Lajić, Séverine Clauin, Tiina Robins, Patrick Vexiau, Hélène Blanché

J Clin Endocrinol Metab· June 2002

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