Found: 24
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Metabolic features of treatment-refractory major depressive disorder with suicidal ideation.
- Published in:
- Translational Psychiatry, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41398-023-02696-9
- By:
- Publication type:
- Article
Selective hypermethylation is evident in small intestine samples from infants with necrotizing enterocolitis.
- Published in:
- Clinical Epigenetics, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13148-022-01266-y
- By:
- Publication type:
- Article
Problem-solving, Adherence to Lifestyle Goals, and Weight Loss Among Individuals Participating in a Weight Loss Study.
- Published in:
- International Journal of Behavioral Medicine, 2021, v. 28, n. 3, p. 328, doi. 10.1007/s12529-020-09922-4
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- Publication type:
- Article
Global hypermethylation of intestinal epithelial cells is a hallmark feature of neonatal surgical necrotizing enterocolitis.
- Published in:
- Clinical Epigenetics, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s13148-020-00983-6
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- Publication type:
- Article
Rare variants and biological pathways identified in treatment‐refractory depression.
- Published in:
- Journal of Neuroscience Research, 2020, v. 98, n. 7, p. 1322, doi. 10.1002/jnr.24609
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- Publication type:
- Article
Chromosome 15q13.3 microduplications are associated with treatment refractory major depressive disorder.
- Published in:
- Genes, Brain & Behavior, 2020, v. 19, n. 5, p. 1, doi. 10.1111/gbb.12628
- By:
- Publication type:
- Article
Genetic association and differential expression of PITX2 with acute appendicitis.
- Published in:
- Human Genetics, 2019, v. 138, n. 1, p. 37, doi. 10.1007/s00439-018-1956-2
- By:
- Publication type:
- Article
Evaluation of disease burden and response to treatment in adults with type 1 gaucher disease using a validated disease severity scoring system (DS3).
- Published in:
- Orphanet Journal of Rare Diseases, 2015, v. 10, n. 1, p. 1, doi. 10.1186/s13023-015-0280-3
- By:
- Publication type:
- Article
Evaluation of disease burden and response to treatment in adults with type 1 Gaucher disease using a validated disease severity scoring system (DS3).
- Published in:
- 2015
- By:
- Publication type:
- journal article
Lymphedema Prevention and Early Intervention: A Worthy Goal.
- Published in:
- Oncology (08909091), 2012, v. 26, n. 3, p. 249
- By:
- Publication type:
- Article
Infant with unusual food reactions (Case Presentation).
- Published in:
- 2011
- By:
- Publication type:
- Case Study
Infant with unusual food reactions (Discussion and Diagnosis).
- Published in:
- Acta Paediatrica, 2011, v. 100, n. 10, p. 1394, doi. 10.1111/j.1651-2227.2011.02319.x
- By:
- Publication type:
- Article
Research Perspectives in Inherited Lymphatic Disease.
- Published in:
- Annals of the New York Academy of Sciences, 2008, v. 1131, p. 134, doi. 10.1196/annals.1413.012
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- Publication type:
- Article
Progress toward the development of a point-of-care photonic crystal ammonia sensor.
- Published in:
- Analytical & Bioanalytical Chemistry, 2006, v. 385, n. 4, p. 678, doi. 10.1007/s00216-006-0453-y
- By:
- Publication type:
- Article
A Genome-Wide Scan for Loci Affecting Normal Adult Height in the Framingham Heart Study.
- Published in:
- Human Heredity, 2003, v. 55, n. 4, p. 191, doi. 10.1159/000073203
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- Publication type:
- Article
Lymphatic endothelial reprogramming of vascular endothelial cells by the Prox-1 homeobox transcription factor.
- Published in:
- EMBO Journal, 2002, v. 21, n. 17, p. 4593, doi. 10.1093/emboj/cdf470
- By:
- Publication type:
- Article
Truncating mutations in FOXC2 cause multiple lymphedema syndromes.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 11, p. 1185, doi. 10.1093/hmg/10.11.1185
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- Publication type:
- Article
Truncating mutations in FOXC2 cause multiple lymphedema syndromes.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 11, p. 1185, doi. 10.1093/hmg/10.11.1185
- By:
- Publication type:
- Article
Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 153, doi. 10.1038/75997
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- Publication type:
- Article
Familial nephrotic syndrome: Clinical spectrum and linkage to chromosome 19q13.
- Published in:
- Kidney International, 2000, v. 57, n. 3, p. 875, doi. 10.1046/j.1523-1755.2000.057003875.x
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- Publication type:
- Article
Hereditary lymphedema: evidence for linkage and genetic heterogeneity.
- Published in:
- Human Molecular Genetics, 1998, v. 7, n. 13
- By:
- Publication type:
- Article
Psychomotor slowing is associated with distal symmetrical polyneuropathy in adults with diabetes mellitus.
- Published in:
- 1992
- By:
- Publication type:
- journal article
Sodium-potassium ATPase activity mediates cyst formation in metanephric organ culture.
- Published in:
- Kidney International, 1985, v. 28, n. 3, p. 447, doi. 10.1038/ki.1985.151
- By:
- Publication type:
- Article
Assessment of stature of children with myelomeningocele, and usefulness of arm-span measurement.
- Published in:
- 1983
- By:
- Publication type:
- journal article