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Cells|March 25, 2022
Molecular Characterization of Portuguese Patients with Hereditary Cerebellar AtaxiaMariana Santos, Joana Damásio, Susana Carmona, et al.
Neuromuscular Disorders : NMD|February 3, 1998
A point mutation in the glycerol kinase gene associated with a deletion in the dystrophin gene in a familial X-linked muscular dystrophy: non-contiguous gene syndrome involving Becker muscular dystrophy and glycerol kinase lociN B Romero, D Récan, O Rigal, et al.
Emerging Infectious Diseases|February 12, 2005
Invasive group A streptococcal infection in high school football players, New York City, 2003Susan E Manning, Elsie Lee, Maribeth Bambino, et al.
European Journal of Haematology|April 9, 2005
Protein deficiency balance as a predictor of clinical outcome in hereditary spherocytosisS Rocha, I Rebelo, E Costa, et al.
BJS Open|March 7, 2021
Radiomics: a new tool to differentiate adrenocortical adenoma from carcinomaF Torresan, F Crimì, F Ceccato, et al.
Cells|November 4, 2020
Blockade of Glial Connexin 43 Hemichannels Reduces Food IntakeFlorent Guillebaud, Manon Barbot, Rym Barbouche, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 25, 2008
Infantile neuroaxonal dystrophy: what's most important for the diagnosis?Inês Carrilho, Manuela Santos, António Guimarães, et al.
European Urology|November 1, 2011
Efficacy and safety of low doses of onabotulinumtoxinA for the treatment of refractory idiopathic overactive bladder: a multicentre, double-blind, randomised, placebo-controlled dose-ranging studyPierre Denys, Loïc Le Normand, Idir Ghout, et al.
Anti-Cancer Drugs|November 9, 2019
Rapid disease progression in patient with mismatch-repair deficiency pituitary ACTH-secreting adenoma treated with checkpoint inhibitor pembrolizumabMario Caccese, Mattia Barbot, Filippo Ceccato, et al.
Frontiers in Endocrinology|October 19, 2020
Practical Considerations for the Management of Cushing's Disease and COVID-19: A Case ReportFederica Beretta, Francesca Dassie, Matteo Parolin, et al.
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