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Annals of Hematology|December 4, 2018
Common fetal hemoglobin variants in Lebanese patients bearing the codon 29 beta gene mutation associated with different thalassemia phenotypesValentina Brancaleoni, Hassan M Moukhadder, Dario Consonni, et al.
Hematology (Amsterdam, Netherlands)|September 10, 2024
Hb SKMC and an unprecedented γδβ-thalassemia: first report from IraqRawand P Shamoon, Amir Charkaneh, Elena Di Pierro, et al.
European Journal of Internal Medicine|June 4, 2020
Hyperhomocysteinemia in patients with acute porphyrias: A potentially dangerous metabolic crossroad?Paolo Ventura, Elena Corradini, Elena Di Pierro, et al.
Diagnostics (Basel, Switzerland)|September 28, 2021
α-Lipoic Acid Improves Hepatic Metabolic Dysfunctions in Acute Intermittent Porphyria: A Proof-of-Concept StudyMiriam Longo, Erika Paolini, Marica Meroni, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|January 21, 2012
Intradural chordoma of the Meckel's cave: a challenging differential diagnosisValeria Barresi, Maria Caffo, Concetta Alafaci, et al.
Pediatric Radiology|November 10, 2012
Pharyngeal enterogenous cyst associated with canalis basilaris medianus in a newbornRosa Morabito, Marcello Longo, Andrea Rossi, et al.
Journal of Clinical Imaging Science|January 23, 2020
Magnetic Resonance Imaging of the Diaphragm: From Normal to Pathologic FindingsGiuseppe Cicero, Silvio Mazziotti, Alfredo Blandino, et al.
European Journal of Neurology|July 10, 2024
A case of frontal lobe seizures with 'dancing-like' semiologyGiorgia Atanasio, Antonio Germanò, Francesca Granata, et al.
Blood Cells, Molecules & Diseases|July 11, 2006
A large deletion on chromosome 11 in acute intermittent porphyriaElena Di Pierro, Valeria Besana, Valeria Moriondo, et al.
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