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The Journal of Clinical Endocrinology and Metabolism|August 6, 2010
Novel heterozygous nonsense GLI2 mutations in patients with hypopituitarism and ectopic posterior pituitary lobe without holoprosencephalyMarcela M França, Alexander A L Jorge, Luciani R S Carvalho, et al.
Cancer Letters|May 26, 2005
Detection of somatic TP53 splice site mutations in diffuse astrocytomasMiyuki Uno, Sueli Mieko Oba-Shinjo, Paulo Henrique de Aguiar, et al.
Neurology|November 21, 2024
Atrophy Patterns in Patients With Multiple Sclerosis With Cognitive Impairment, Fatigue, and Mood DisordersCarolina de Medeiros Rimkus, Mariana Penteado Nucci, Isabella B Avolio, et al.
Arquivos De Neuro-Psiquiatria|May 11, 2017
Home-based exercise program in TSP/HAM individuals: a feasibility and effectiveness studyLívia D Facchinetti, Abelardo Q Araújo, Marcus Tt Silva, et al.
Epilepsy Research|September 28, 2014
Diffusion abnormalities of the corpus callosum in patients with malformations of cortical development and epilepsyCeli S Andrade, Claudia C Leite, Maria C G Otaduy, et al.
The Journal of Clinical Endocrinology and Metabolism|November 5, 2002
Pituitary magnetic resonance imaging and function in patients with growth hormone deficiency with and without mutations in GHRH-R, GH-1, or PROP-1 genesMaria Geralda F Osorio, Suemi Marui, Alexander A L Jorge, et al.
Revista Brasileira De Psiquiatria (Sao Paulo, Brazil : 1999)|October 5, 2017
Support vector machine-based classification of neuroimages in Alzheimer's disease: direct comparison of FDG-PET, rCBF-SPECT and MRI data acquired from the same individualsLuiz K Ferreira, Jane M Rondina, Rodrigo Kubo, et al.
Clinics (Sao Paulo, Brazil)|December 17, 2020
Differences in Total Brain Volume between Sexes in a Cognitively Unimpaired Elderly PopulationMarina Buchpiguel, Pedro Rosa, Paula Squarzoni, et al.
Pituitary|October 16, 2014
Frequent development of combined pituitary hormone deficiency in patients initially diagnosed as isolated growth hormone deficiency: a long term follow-up of patients from a single centerAline P Otto, Marcela M França, Fernanda A Correa, et al.
Pediatric Radiology|March 8, 2005
Merosin-deficient congenital muscular dystrophy (CMD): a study of 25 Brazilian patients using MRIClaudia C Leite, Leandro T Lucato, Maria G M Martin, et al.
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