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Caries Research|May 15, 2016
Family-Based Genetic Association for Molar-Incisor HypomineralizationFabiano Jeremias, Ricardo A G Pierri, Juliana F Souza, et al.
International Journal of Cardiology|November 26, 2024
Differences between MINOCA and type 2 myocardial infarction: An ITALIAN observational studyAneta Aleksova, Alessandra Lucia Fluca, Milijana Janjusevic, et al.
Blood|October 24, 2002
CTLA-4 is not restricted to the lymphoid cell lineage and can function as a target molecule for apoptosis induction of leukemic cellsMaria Pia Pistillo, Pier Luigi Tazzari, Giulio Lelio Palmisano, et al.
American Journal of Medical Genetics. Part A|January 13, 2022
Expanded cardiovascular phenotype of Myhre syndrome includes tetralogy of Fallot suggesting a role for SMAD4 in human neural crest defectsGerarda Cappuccio, Nicola Brunetti-Pierri, Paul Clift, et al.
American Journal of Human Genetics|June 11, 2019
Pathogenic Variants in NUP214 Cause "Plugged" Nuclear Pore Channels and Acute Febrile EncephalopathyBoris Fichtman, Tamar Harel, Nitzan Biran, et al.
Leukemia Research|July 29, 2011
Weekly standard doses of rh-EPO are highly effective for the treatment of anemic patients with low-intermediate 1 risk myelodysplastic syndromesEnrico Balleari, Marino Clavio, Eleonora Arboscello, et al.
Cellular and Molecular Gastroenterology and Hepatology|June 5, 2026
Loss of the mechanistic target of rapamycin complexes 1 (mTORC1) causes a lethal alpha-1 antitrypsin deficiency associated liver diseaseLisa Bewersdorf, Sophie Haber, Ines Volkert, et al.
Genes|September 28, 2024
Uncovering a Genetic Diagnosis in a Pediatric Patient by Whole Exome Sequencing: A Modeling Investigation in Wiedemann-Steiner SyndromeIghli di Bari, Caterina Ceccarini, Maria Curcetti, et al.
JACC. Cardiovascular Interventions|September 22, 2014
Cerebrovascular events post-transcatheter aortic valve replacement in a large cohort of patients: a FRANCE-2 registry substudyDidier Tchetche, Bruno Farah, Leonardo Misuraca, et al.
Birth Defects Research|June 18, 2022
Genotype-phenotype spectrum and correlations in Xia-Gibbs syndrome: Report of five novel cases and literature reviewFerruccio Romano, Mariateresa Falco, Gerarda Cappuccio, et al.
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