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Obstetrical & Gynecological Survey|November 20, 2008
Mutations and polymorphisms of the FSH receptor (FSHR) gene: clinical implications in female fecundity and molecular biology of FSHR protein and geneCristina Lussiana, Benedetta Guani, Caterina Mari, et al.
Journal of Assisted Reproduction and Genetics|July 28, 2011
FSH-receptor Ala307Thr polymorphism is associated to polycystic ovary syndrome and to a higher responsiveness to exogenous FSH in Italian womenElisabetta Dolfin, Benedetta Guani, Cristina Lussiana, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|June 6, 2009
Ovarian hyper-stimulation syndrome after spontaneous conceptionCristina Lussiana, Benedetta Guani, Gabriella Restagno, et al.
Clinical Chemistry and Laboratory Medicine|October 30, 2013
Identification of an 18 bp deletion in the TWIST1 gene by CO-amplification at lower denaturation temperature-PCR (COLD-PCR) for non-invasive prenatal diagnosis of craniosynostosis: first case reportSilvia Galbiati, Stefania Stenirri, Luca Sbaiz, et al.
The Journal of Urology|July 12, 2005
Low renin-angiotensin system activity gene polymorphism and dysplasia associated with posterior urethral valvesLicia Peruzzi, Federica Lombardo, Alessandro Amore, et al.
Expert Opinion on Biological Therapy|April 18, 2012
Fetal DNA in maternal plasma: a noninvasive tool for prenatal diagnosis of beta-thalassemiaSilvia Galbiati, Angela Brisci, Francesco Damin, et al.
Autoimmunity Reviews|December 11, 2012
Lab-on-a-chip: emerging analytical platforms for immune-mediated diseasesElisa Menegatti, Daniela Berardi, Margherita Messina, et al.
The Journal of Biological Chemistry|August 10, 2004
Effect of ryanodine receptor mutations on interleukin-6 release and intracellular calcium homeostasis in human myotubes from malignant hyperthermia-susceptible individuals and patients affected by central core diseaseSylvie Ducreux, Francesco Zorzato, Clemens Müller, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|February 15, 2008
The rare G93D mutation causes a slowly progressing lower motor neuron diseaseGabriella Restagno, Federica Lombardo, Luca Sbaiz, et al.
Clinical Chemistry and Laboratory Medicine|September 5, 2009
Application of pyrosequencing to the identification of sequence variations in the cystic fibrosis transmembrane conductance regulator geneCaterina Mari, Francesca Bruno, Silvia Galbiati, et al.
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