Found: 9
Select item for more details and to access through your institution.
Novel ERLIN2 variant expands the phenotype of Spastic Paraplegia 18.
- Published in:
- Neurological Sciences, 2024, v. 45, n. 6, p. 2705, doi. 10.1007/s10072-023-07271-0
- By:
- Publication type:
- Article
Reconsidering the Association Between the Major Histocompatibility Complex and Bipolar Disorder.
- Published in:
- Journal of Molecular Neuroscience, 2012, v. 47, n. 1, p. 26, doi. 10.1007/s12031-011-9656-6
- By:
- Publication type:
- Article
Loss-of-function mutation in inositol monophosphatase 1 (IMPA1) results in abnormal synchrony in resting-state EEG.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Reliability of information on people with disabilities gathered by community health workers in highly consanguineous communities of Northeastern Brazil.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Neuropsychological Characterization of Autosomal Recessive Intellectual Developmental Disorder 59 Associated with IMPA1 (MRT59).
- Published in:
- Brain Sciences (2076-3425), 2023, v. 13, n. 7, p. 1048, doi. 10.3390/brainsci13071048
- By:
- Publication type:
- Article
SOCIO-DEMOGRAPHIC PROFILE AND THE LICIT AND ILLICIT DRUGS USE AMONG SECONDARY EDUCATION STUDENTS.
- Published in:
- SMAD Revista Electronica Salud Mental, Alcohol y Drogas, 2013, v. 9, n. 1, p. 3
- By:
- Publication type:
- Article
Different gene expression profiles in iPSC-derived motor neurons from ALS8 patients with variable clinical courses suggest mitigating pathways for neurodegeneration.
- Published in:
- Human Molecular Genetics, 2020, v. 29, n. 9, p. 1465, doi. 10.1093/hmg/ddaa069
- By:
- Publication type:
- Article
Overexpression of KLC2 due to a homozygous deletion in the non-coding region causes SPOAN syndrome.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 24, p. 6877, doi. 10.1093/hmg/ddv388
- By:
- Publication type:
- Article
Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations.
- Published in:
- Clinical Endocrinology, 2017, v. 87, n. 6, p. 725, doi. 10.1111/cen.13430
- By:
- Publication type:
- Article