Found: 23
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Vulnerability in Children with Celiac Disease: Findings from a Scoping Review.
- Published in:
- Children, 2024, v. 11, n. 6, p. 729, doi. 10.3390/children11060729
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- Publication type:
- Article
Gastroenterological Manifestations of Immunoglobulin G Subclass 4-Related Disease—Epidemiology, Clinical Manifestations, Diagnosis and Treatment.
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- Life (2075-1729), 2023, v. 13, n. 8, p. 1725, doi. 10.3390/life13081725
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- Publication type:
- Article
O Sofrimento Psíquico: Influências identificadas acerca do processo de escolha profissional em jovens.
- Published in:
- Id on Line. Revista de Psicologia, 2023, v. 17, n. 66, p. 504, doi. 10.14295/idonline.v17i66.3788
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- Publication type:
- Article
Vulnerability in Children with Celiac Disease: A Scoping Review Protocol.
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- Nursing Reports, 2022, v. 12, n. 4, p. 685, doi. 10.3390/nursrep12040068
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- Publication type:
- Article
Arginase 1 deficiency presenting as complicated hereditary spastic paraplegia.
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- Cold Spring Harbor Molecular Case Studies, 2022, v. 8, n. 6, p. 1, doi. 10.1101/mcs.a006232
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- Article
A TRADIÇÃO PROFÉTICA NO ANTIGO TESTAMENTO E SUA INFLUÊNCIA NA IDENTIDADE DE ISRAEL.
- Published in:
- Protestantismo em Revista, 2022, v. 48, n. 1, p. 29, doi. 10.22351/nepp.v45i2
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- Publication type:
- Article
Apraxia of Eyelid Opening and Blepharospasm in Two Spinocerebellar Ataxia Type 3 Patients.
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- Tremor & Other Hyperkinetic Movements, 2022, v. 12, p. 1, doi. 10.5334/tohm.677
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- Publication type:
- Article
Efeitos abrasivos produzidos por um dentifrício à base de carvão.
- Published in:
- Stomatos, 2020, v. 26, n. 51, p. 77
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- Publication type:
- Article
A novel complex neurological phenotype due to a homozygous mutation in FDX2.
- Published in:
- 2018
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- Publication type:
- journal article
A Política Nacional de Educação Permanente em Saúde nas Escolas de Saúde Pública: reflexões a partir da prática.
- Published in:
- Revista Ciência & Saúde Coletiva, 2017, v. 22, n. 5, p. 1489, doi. 10.1590/1413-81232017225.33222016
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- Publication type:
- Article
The National Permanent Health Education Policy in Public Health Schools: reflections from practice.
- Published in:
- Revista Ciência & Saúde Coletiva, 2017, v. 22, n. 5, p. 1489, doi. 10.1590/1413-81232017225.33222016
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- Publication type:
- Article
Inferring paternal history of rural African-derived Brazilian populations from Y chromosomes.
- Published in:
- American Journal of Human Biology, 2017, v. 29, n. 2, p. n/a, doi. 10.1002/ajhb.22930
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- Publication type:
- Article
A novel GFAP mutation in a type II (late-onset) Alexander disease patient.
- Published in:
- 2016
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- Publication type:
- Letter
Parents' conceptions of their homework involvement in elementary school.
- Published in:
- Psicothema, 2015, v. 27, n. 2, p. 159, doi. 10.7334/psicothema2014.210
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- Publication type:
- Article
RETIREMENT IN NURSING: A REVIEW OF THE LITERATURE.
- Published in:
- 2014
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- Publication type:
- Journal Article
Nerve conduction studies in spastic paraplegia, optic atrophy, and neuropathy (SPOAN) syndrome.
- Published in:
- Muscle & Nerve, 2014, v. 49, n. 1, p. 131, doi. 10.1002/mus.24087
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- Publication type:
- Article
ACIDENTES COM MATERIAL BIOLÓGICO EM TRABALHADORES.
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- Rev Rene, 2013, v. 14, n. 5, p. 971, doi. 10.15253/2175-6783.20130005000014
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- Publication type:
- Article
ACCIDENTS WITH BIOLOGICAL MATERIAL IN WORKERS.
- Published in:
- 2013
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- Publication type:
- Journal Article
PRACTICE OF PERMANENT EDUCATION BY NURSING CARE IN HEALTH SERVICES.
- Published in:
- Journal of Nursing UFPE / Revista de Enfermagem UFPE, 2013, v. 7, n. 2, p. 598, doi. 10.5205/reuol.3073-24791-1-LE.0702201335
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- Publication type:
- Article
CONSUMO ALIMENTAR E ESTADO NUTRICIONAL DE PRÉ-ESCOLARES DE UM CENTRO DE EDUCAÇÃO INFANTIL DO MUNICÍPIO DE SÃO PAULO.
- Published in:
- Brazilian Journal of Food & Nutrition / Alimentos e Nutrição, 2010, v. 21, n. 3, p. 407
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- Publication type:
- Article
Spastic Paraplegia, Optic Atrophy, and Neuropathy: New Observations, Locus Refinement, and Exclusion of Candidate Genes.
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- Annals of Human Genetics, 2009, v. 73, n. 3, p. 382, doi. 10.1111/j.1469-1809.2009.00507.x
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- Publication type:
- Article
Reevaluation of a large family defines a new locus for X-linked recessive pure spastic paraplegia (SPG34) on chromosome Xq25.
- Published in:
- 2008
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- Publication type:
- Letter
Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration.
- Published in:
- EMBO Reports, 2007, v. 8, n. 7, p. 691, doi. 10.1038/sj.embor.7401001
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- Publication type:
- Article