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Mutation Research|April 30, 2013
Fosfomycin increases chromosome instability in lymphocytes from Fanconi Anemia patientsRosa Sousa, Filipa Ponte, Sara Teixeira, et al.
Acta Medica Portuguesa|April 12, 2003
[Glucose-6-phosphate dehydrogenase deficiency, neonatal hyperbilirubinemia and Gilbert syndrome]Elísio Costa, Emilia Vieira, Esmeralda Cleto, et al.
Clinical and Laboratory Haematology|July 29, 2004
Coexistence of congenital red cell pyruvate kinase and band 3 deficiencyR Branca, E Costa, S Rocha, et al.
Development and Psychopathology|October 16, 2012
Childhood adversity and DNA methylation of genes involved in the hypothalamus-pituitary-adrenal axis and immune system: whole-genome and candidate-gene associationsJohanna Bick, Oksana Naumova, Scott Hunter, et al.
Expert Review of Endocrinology & Metabolism|March 6, 2023
Knowing when to discontinue Temozolomide therapy in responding aggressive pituitary tumors and carcinomas: a systematic review and Padua (Italy) case seriesMarta Padovan, Giulia Cerretti, Mario Caccese, et al.
Genomics|October 1, 1989
Analysis of molecular deletions with cDNA probes in patients with Duchenne and Becker muscular dystrophiesH Gilgenkrantz, J Chelly, M Lambert, et al.
Endocrine|December 16, 2014
The role of an acute pasireotide suppression test in predicting response to treatment in patients with Cushing's disease: findings from a pilot studyL Trementino, M Zilio, G Marcelli, et al.
Blood|February 9, 2000
Glucose-6-phosphate dehydrogenase aveiro: a de novo mutation associated with chronic nonspherocytic hemolytic anemiaE Costa, J M Cabeda, E Vieira, et al.
Disability and Rehabilitation|May 17, 2023
Effects of compression garments on balance in hypermobile Ehlers-Danlos syndrome: a randomized controlled trialKarelle Benistan, Malika Foy, Fabrice Gillas, et al.
Anales Espanoles De Pediatria|June 4, 2002
[Transient erythroblastopenia in the context of Epstein-Barr virus infection]M Sameiro Barreirinho, M Lopes Guerra, E Sousa Costa, et al.
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