Concepedia

Mariateresa Di Stazio

MD

13

Publications

840

Citations

12

H-Index

2004

Active since

Affiliations

IRCCS Materno Infantile Burlo Garofolo(Current)

University of Trieste

University of Pavia

Istituti di Ricovero e Cura a Carattere Scientifico

University of Bologna

Mariateresa Di Stazio is an author at IRCCS Materno Infantile Burlo Garofolo specializing in medicine, genetics, and auditory research.

Top concepts

MedicineGeneticsArtsAudiologyHearing LossAuditory ResearchAuditory PhysiologyPathologyCovid-19Hematology

Publications per year

2004–2021

13

Publications

13

Mutations in the 5′ UTR of ANKRD26, the Ankirin Repeat Domain 26 Gene, Cause an Autosomal-Dominant Form of Inherited Thrombocytopenia, THC2

Tommaso Pippucci, Anna Savoia, Silverio Perrotta et al. · The American Journal of Human Genetics · 2011 · 217 citations · Full text

Thrombopoiesis, Autoimmune Disease, Genetic Disorder +6

Nonmuscle Myosin Heavy-Chain Gene MYH14 Is Expressed in Cochlea and Mutated in Patients Affected by Autosomal Dominant Hearing Impairment (DFNA4)

Francesca Donaudy, Rik L. Snoeckx, Markus Pfister et al. · The American Journal of Human Genetics · 2004 · 167 citations · Full text

Patients Affected, Genetic Disorder, Genetics +8

Clinical and genetic aspects of Bernard-Soulier syndrome: searching for genotype/phenotype correlations

Anna Savoia, Alessandro Pastore, Daniela De Rocco et al. · Haematologica · 2010 · 105 citations · Full text

Correlation between the clinical phenotype of MYH9 -related disease and tissue distribution of class II nonmuscle myosin heavy chains

Valeria Marigo, Alessandra Nigro, Alessandro Pecci et al. · Genomics · 2004 · 79 citations · Full text

Disease Mechanism, Skeletal Muscle, Medicine +7

Application of a diagnostic algorithm for inherited thrombocytopenias to 46 consecutive patients.

Patrizia Noris, Alessandro Pecci, Filomena Di Bari et al. · PubMed · 2004 · 69 citations

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