Found: 15
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Endovascular treatment of patients with stroke caused by anterior cerebral artery occlusions.
- Published in:
- Acta Neurologica Belgica, 2024, v. 124, n. 2, p. 621, doi. 10.1007/s13760-023-02395-8
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- Publication type:
- Article
Systematic Review - Combining Neuroprotection With Reperfusion in Acute Ischemic Stroke.
- Published in:
- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.840892
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- Publication type:
- Article
Prenatal exome sequencing: A useful tool for the fetal neurologist.
- Published in:
- Clinical Genetics, 2022, v. 101, n. 1, p. 65, doi. 10.1111/cge.14070
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- Publication type:
- Article
Intracerebral hemorrhage in a neonate with an intragenic COL4A2 duplication.
- Published in:
- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 2, p. 571, doi. 10.1002/ajmg.a.61988
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- Publication type:
- Article
Incidence and outcome of acquired demyelinating syndromes in Dutch children: update of a nationwide and prospective study.
- Published in:
- Journal of Neurology, 2018, v. 265, n. 6, p. 1310, doi. 10.1007/s00415-018-8835-6
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- Publication type:
- Article
Nitric Oxide Synthase Inhibition as a Neuroprotective Strategy Following Hypoxic-Ischemic Encephalopathy: Evidence From Animal Studies.
- Published in:
- Frontiers in Neurology, 2018, p. 1, doi. 10.3389/fneur.2018.00258
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- Publication type:
- Article
Genotype-phenotype correlation in ATAD3A deletions: not just of scientific relevance.
- Published in:
- 2017
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- Publication type:
- letter
Fetal brain imaging in isolated congenital heart defects - a systematic review and meta-analysis.
- Published in:
- 2016
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- Publication type:
- journal article
Polyhydramnios and cerebellar atrophy: a prenatal presentation of mitochondrial encephalomyopathy caused by mutations in the FBXL4 gene.
- Published in:
- Clinical Case Reports, 2016, v. 4, n. 4, p. 425, doi. 10.1002/ccr3.511
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- Publication type:
- Article
Clinical and molecular characterization of an infant with a tandem duplication and deletion of 19p13.
- Published in:
- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 8, p. 1884, doi. 10.1002/ajmg.a.37076
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- Publication type:
- Article
Chronological changes of the amplitude‐integrated EEG in a neonate with molybdenum cofactor deficiency.
- Published in:
- Journal of Inherited Metabolic Disease, 2010, v. 33, p. 401, doi. 10.1007/s10545-010-9198-z
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- Publication type:
- Article
Chronological changes of the amplitude-integrated EEG in a neonate with molybdenum cofactor deficiency.
- Published in:
- Journal of Inherited Metabolic Disease, 2010, v. 33, p. S401, doi. 10.1007/s10545-010-9198-z
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- Publication type:
- Article
Abdominal decompression for intra-abdominal hypertension after simultaneous pancreas–kidney transplantation.
- Published in:
- Clinical Transplantation, 2010, v. 24, n. 1, p. 118, doi. 10.1111/j.1399-0012.2009.01147.x
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- Publication type:
- Article
Variable phenotypes associated with 10q23 microdeletions involving the PTEN and BMPR1A genes.
- Published in:
- Clinical Genetics, 2008, v. 74, n. 2, p. 145, doi. 10.1111/j.1399-0004.2008.01026.x
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- Publication type:
- Article
Long-term neuroprotection with 2-iminobiotin, an inhibitor of neuronal and inducible nitric oxide synthase, after cerebral hypoxia–ischemia in neonatal rats.
- Published in:
- Journal of Cerebral Blood Flow & Metabolism, 2005, v. 25, n. 1, p. 67, doi. 10.1038/sj.jcbfm.9600007
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- Publication type:
- Article