Found: 22
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Chocolate flavanols and skin photoprotection: a parallel, double-blind, randomized clinical trial.
- Published in:
- Nutrition Journal, 2014, v. 13, p. 200, doi. 10.1186/1475-2891-13-66
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- Article
Chocolate flavanols and skin photoprotection: a parallel, double-blind, randomized clinical trial.
- Published in:
- 2014
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- Publication type:
- journal article
Blood pressure and endothelial function in healthy, pregnant women after acute and daily consumption of flavanol-rich chocolate: a pilot, randomized controlled trial.
- Published in:
- Nutrition Journal, 2013, v. 12, p. 1, doi. 10.1186/1475-2891-12-41
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- Article
Blood pressure and endothelial function in healthy, pregnant women after acute and daily consumption of flavanol-rich chocolate: a pilot, randomized controlled trial.
- Published in:
- 2013
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- Publication type:
- journal article
Plasma organochlorine concentrations and bone ultrasound measurements: a cross-sectional study in peri-and postmenopausal Inuit women from Greenland.
- Published in:
- Environmental Health: A Global Access Science Source, 2006, v. 5, p. 33, doi. 10.1186/1476-069X-5-33
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- Article
A Frequent Regulatory Variant of the Estrogen-Related Receptor α Gene Associated With BMD in French-Canadian Premenopausal Women.
- Published in:
- Journal of Bone & Mineral Research, 2005, v. 20, n. 6, p. 938, doi. 10.1359/JBMR.050203
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- Article
Connexin30 mutations responsible for hidrotic ectodermal dysplasia cause abnormal hemichannel activity.
- Published in:
- Human Molecular Genetics, 2004, v. 13, n. 16, p. 1703, doi. 10.1093/hmg/ddh191
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- Publication type:
- Article
Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 18, p. 2369, doi. 10.1093/hmg/ddg235
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- Publication type:
- Article
Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) aremutated in non-bullous congenital ichthyosiform erythroderma (NCIE)linked to chromosome 17p13.1.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 1, p. 107, doi. 10.1093/hmg/11.1.107
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- Article
Novel Point Mutations, Deletions, and Polymorphisms in the Cathepsin C Gene in Nine Families from Europe and North Africa with Papillon–Lefèvre Syndrome.
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- Journal of Investigative Dermatology, 2001, v. 117, n. 6, p. 1657, doi. 10.1046/j.0022-202X.2001.01595.x
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- Publication type:
- Article
Mutations in GJB6 cause hidrotic ectodermal dysplasia.
- Published in:
- Nature Genetics, 2000, v. 26, n. 2, p. 142, doi. 10.1038/79851
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- Article
The Association Between Heel Ultrasound and Hormone Replacement Therapy Is Modulated by a Two-Locus Vitamin D and Estrogen Receptor Genotype.
- Published in:
- Journal of Bone & Mineral Research, 2000, v. 15, n. 6, p. 1076, doi. 10.1359/jbmr.2000.15.6.1076
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- Publication type:
- Article
Prenatal diagnosis of pyloric atresia-junctional epidermolysis bullosa syndrome in a fetus not known to be at risk.
- Published in:
- 2000
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- Publication type:
- journal article
A Novel Homozygous Mutation Affecting Integrin α6 in a Case of Junctional Epidermolysis Bullosa with Pyloric Atresia Detected In Utero by Ultrasound Examination.
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- Journal of Investigative Dermatology, 1998, v. 111, n. 5, p. 914, doi. 10.1046/j.1523-1747.1998.00373.x
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- Article
Predominance of the Recurrent Mutation R635X in the LAMB3 Gene in European Patients with Herlitz Junctional Epidermolysis Bullosa Has Implications for Mutation Detection Strategy.
- Published in:
- 1997
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- Publication type:
- Report
Mapping of a Second Locus for Lamellar Ichthyosis to Chromosome 2q33–35.
- Published in:
- Human Molecular Genetics, 1996, v. 5, n. 4, p. 555, doi. 10.1093/hmg/5.4.555
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- Article
Prenatal diagnosis of Herlitz junctional epidermolysis bullosa by amniocentesis.
- Published in:
- 1995
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- Publication type:
- journal article
Autosomal recessive lamellar ichthyosis: identification of a new mutation in transglutaminase 1 and evidence for genetic heterogeneity.
- Published in:
- Human Molecular Genetics, 1995, v. 4, n. 8, p. 1391
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- Publication type:
- Article
DNA-Based Prenatal Diagnosis of Generalized Recessive Dystrophic Epidermolysis Bullosa in Six Pregnancies at Risk for Recurrence.
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- Journal of Investigative Dermatology, 1995, v. 104, n. 4, p. 456, doi. 10.1111/1523-1747.ep12605893
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- Publication type:
- Article
Poikiloderma of Theresa Kindler: Report of a Case with Ultrastructural Study, and Review of the Literature.
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- Pediatric Dermatology, 1989, v. 6, n. 2, p. 82, doi. 10.1111/j.1525-1470.1989.tb01003.x
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- Article
Hereditary epidermolytic palmoplantar keratoderma associated with breast and ovarian cancer in a large kindred.
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- British Journal of Dermatology, 1987, v. 117, n. 3, p. 363, doi. 10.1111/j.1365-2133.1987.tb04144.x
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- Publication type:
- Article
Clinical Observation, Virologic Studies, and Treatment Trials in Patients with Epidermodysplasia Verruciformis, a Disease Induced by Specific Human Papillomaviruses.
- Published in:
- Journal of Investigative Dermatology, 1984, v. 83, p. 18s, doi. 10.1038/jid.1984.15
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- Publication type:
- Article