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Congenital Hyperinsulinism in Brazilian Neonates: A Study of Histology, KATP Channel Genes, and Proliferation of β Cells.
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- Pediatric & Developmental Pathology, 2010, v. 13, n. 5, p. 375, doi. 10.2350/08-12-0578.1
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- Article
CONGENITAL HYPERINSULINISM IN BRAZILIAN NEONATES: A STUDY OF HISTOLOGY, KATP CHANNEL GENES AND PROLIFERATION OF β-CELLS.
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- Pediatric & Developmental Pathology, 2010, v. 13, n. 3, p. 1
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- Article
Protein modeling.
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- Physical Sciences Reviews, 2023, v. 8, n. 4, p. 567, doi. 10.1515/psr-2018-0161
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- Article
Methodology for Location of Shorelines using 3D-GPS Positioning: A Case Study at Saua"ui Beach, Northeast Brazil.
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- Journal of Coastal Research, 2009, v. 25, n. 4, p. 1052, doi. 10.211/08-1108.1
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- Article
The laparoscopic management of intersex patients: the preferred approach.
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- BJU International, 2005, v. 95, n. 6, p. 863, doi. 10.1111/j.1464-410X.2005.05417.x
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- Article
Surgery for adrenal tumours with thrombus in the supra-diaphragmatic infra-atrial inferior vena cava, with no cardiopulmonary bypass.
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- BJU International, 2004, v. 94, n. 1, p. 70, doi. 10.1111/j.1464-410X.2004.04903.x
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- Article
Epidemiologic and Clinical Progression of Lobomycosis among Kaiabi Indians, Brazil, 1965-2019.
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- 2020
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- journal article
Influencia del procesado industrial sobre las características químico-físicas y contenido en lípidos y antioxidantes del salvado de arroz.
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- Grasas y Aceites, 2009, v. 60, n. 2, p. 184, doi. 10.3989/gya.075108
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- Article
Seasonal variations in aerosols and atmospheric transmission at Mauna Loa Observatory.
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- Journal of Geophysical Research. Oceans, 1981, v. 86, n. C8, p. 7395, doi. 10.1029/JC086iC08p07395
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- Article
Secondary Metabolites with Antioxidant Activities for the Putative Treatment of Amyotrophic Lateral Sclerosis (ALS): "Experimental Evidences".
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- Oxidative Medicine & Cellular Longevity, 2020, p. 1, doi. 10.1155/2020/5642029
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- Article
Identification of New Targets and the Virtual Screening of Lignans against Alzheimer's Disease.
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- Oxidative Medicine & Cellular Longevity, 2020, p. 1, doi. 10.1155/2020/3098673
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- Article
Methylome profiling of healthy and central precocious puberty girls.
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- Clinical Epigenetics, 2018, v. 10, n. 1, p. N.PAG, doi. 10.1186/s13148-018-0581-1
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- Article
Identification of the first homozygous 1‐bp deletion in <italic>GDF9</italic> gene leading to primary ovarian insufficiency by using targeted massively parallel sequencing.
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- Clinical Genetics, 2018, v. 93, n. 2, p. 408, doi. 10.1111/cge.13156
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- Article
Molecular analysis of CYP21A2 can optimize the follow-up of positive results in newborn screening for congenital adrenal hyperplasia.
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- Clinical Genetics, 2009, v. 76, n. 6, p. 503, doi. 10.1111/j.1399-0004.2009.01274.x
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- Article
The occurrence of the Indo-Pacific swimming crab Scylla serrata (Forskål, 1775) in the Southwestern Atlantic (Crustacea: Brachyura: Portunidae).
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- Aquatic Invasions, 2011, v. 6, p. S49, doi. 10.3391/ai.2011.6.S1.011
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- Article
Avocado Oil Incorporated in Ultrafine Zein Fibers by Electrospinning.
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- Food Biophysics, 2019, v. 14, n. 4, p. 383, doi. 10.1007/s11483-019-09587-x
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- Article
A meiotic recombination in a new isolated familial somatotropinoma kindred.
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- European Journal of Endocrinology, 2004, v. 150, n. 5, p. 0643
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- Article
GH Treatment in Children of Normal Height.
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- Journal of Clinical Endocrinology & Metabolism, 2024, v. 109, n. 10, p. e1955, doi. 10.1210/clinem/dgae457
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- Article
Evidence for a Founder Effect of SDHB Exon 1 Deletion in Brazilian Patients With Paraganglioma.
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- Journal of Clinical Endocrinology & Metabolism, 2023, v. 108, n. 8, p. 2105, doi. 10.1210/clinem/dgad028
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- Article
Clinical and Genetic Characterization of Familial Central Precocious Puberty.
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- Journal of Clinical Endocrinology & Metabolism, 2023, v. 108, n. 7, p. 1758, doi. 10.1210/clinem/dgac763
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- Article
Primary Adrenal Insufficiency Due to Bilateral Adrenal Infarction in COVID-19.
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- Journal of Clinical Endocrinology & Metabolism, 2022, v. 107, n. 1, p. e394, doi. 10.1210/clinem/dgab557
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- Article
Steroid Screening Tools Differentiating Nonclassical Congenital Adrenal Hyperplasia and Polycystic Ovary Syndrome.
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- 2020
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- Publication type:
- journal article
Plasma Renin Measurements are Unrelated to Mineralocorticoid Replacement Dose in Patients With Primary Adrenal Insufficiency.
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- 2019
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- Publication type:
- journal article
Synthesis, Structure-Activity Relationships (SAR) and in Silico Studies of Coumarin Derivatives with Antifungal Activity.
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- International Journal of Molecular Sciences, 2013, v. 14, n. 1, p. 1293, doi. 10.3390/ijms14011293
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- Article
Pulsatile Secretion of Serum Gonadotropins in Hirsute Women with and without Polycystic Ovarian Syndrome.
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- Annals of the New York Academy of Sciences, 1993, v. 687, n. 1, p. 136, doi. 10.1111/j.1749-6632.1993.tb43862.x
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- Article
Characterization of hydroxyaromatic compounds in vegetable oils by capillary electrophoresis with direct injection in an oil-miscible KOH/propanol/methanol medium.
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- Electrophoresis, 2005, v. 26, n. 17, p. 3307
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- Article
Growth hormone pharmacogenetics: the interactive effect of a microsatellite in the IGF1 promoter region with the GHR-exon 3 and −202 A/C IGFBP3 variants on treatment outcomes of children with severe GH deficiency.
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- Pharmacogenomics Journal, 2012, v. 12, n. 5, p. 439, doi. 10.1038/tpj.2011.13
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- Article
New species of the genus Spectracanthicus (Loricariidae, Hypostominae, Ancistrini) from the Rio Javaés (Rio Araguaia basin), with a description of gross brain morphology.
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- Journal of Fish Biology, 2018, v. 92, n. 2, p. 438, doi. 10.1111/jfb.13526
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- Article
Genealogy of the nuclear β-fibrinogen locus in a highly structured lizard species: comparison with mtDNA and evidence for intragenic recombination in the hybrid zone.
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- Heredity, 2006, v. 96, n. 6, p. 454, doi. 10.1038/sj.hdy.6800823
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- Article
Central Precocious Puberty Caused by a Heterozygous Deletion in the <bold>MKRN3</bold> Promoter Region.
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- Neuroendocrinology, 2018, v. 107, n. 2, p. 127, doi. 10.1159/000490059
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- Article
Long-Term Outcomes of Patients with Central Precocious Puberty due to Hypothalamic Hamartoma after GnRHa Treatment: Anthropometric, Metabolic, and Reproductive Aspects.
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- Neuroendocrinology, 2018, v. 106, n. 3, p. 203, doi. 10.1159/000477584
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- Article
High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic.
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- Neuroendocrinology, 2017, v. 105, n. 1, p. 17, doi. 10.1159/000446963
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- Article
Growth standards of patients with Noonan and Noonan-like syndromes with mutations in the RAS/MAPK pathway.
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- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 11, p. 2700, doi. 10.1002/ajmg.a.35519
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- Article
Corrigendum: Synthesis and Evaluation of 2‐Aminothiophene Derivatives as Staphylococcus aureus Efflux Pump Inhibitors.
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- ChemMedChem, 2021, v. 16, n. 10, p. 1680, doi. 10.1002/cmdc.2020100124
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- Article
Synthesis and Evaluation of 2‐Aminothiophene Derivatives as Staphylococcus aureus Efflux Pump Inhibitors.
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- ChemMedChem, 2020, v. 15, n. 8, p. 716, doi. 10.1002/cmdc.201900688
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- Article
Finite Element Analysis of Experimentally Tested Concrete Slabs Subjected to Airblast.
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- Defence Science Journal, 2021, v. 71, n. 5, p. 630, doi. 10.14429/dsj.71.15576
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- Article
Comparison of Predicted and Experimental Behaviour of RC Slabs Subjected to Blast using SDOF Analysis.
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- Defence Science Journal, 2018, v. 68, n. 2, p. 138, doi. 10.14429/dsj.68.11682
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- Article
Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty.
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- Journal of Clinical Endocrinology & Metabolism, 2017, p. 1557, doi. 10.1210/jc.2016-3677
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- Article
Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty.
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- 2017
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- Publication type:
- journal article
Successful Live Birth in a Woman With 17α-Hydroxylase Deficiency Through IVF Frozen-Thawed Embryo Transfer.
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- 2016
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- Publication type:
- journal article
Genetic Predictors of Long-Term Response to Growth Hormone (GH) Therapy in Children With GH Deficiency and Turner Syndrome: The Influence of a SOCS2 Polymorphism.
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- 2014
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- Publication type:
- Journal Article
Central precocious puberty that appears to be sporadic caused by paternally inherited mutations in the imprinted gene makorin ring finger 3.
- Published in:
- 2014
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- Publication type:
- journal article
Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency.
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- Journal of Clinical Endocrinology & Metabolism, 2011, v. 96, n. 9, p. E1457, doi. 10.1210/jc.2011-0170
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- Publication type:
- Article
Zinc does not inhibit prolactin secretion during insulin-induced hypoglycemia in normal men.
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- Trace Elements & Electrolytes, 2006, v. 23, n. 1, p. 50, doi. 10.5414/TEP23050
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- Article
Lack of inhibitory effect of zinc on prolactin secretion induced by cimetidine.
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- Trace Elements & Electrolytes, 2005, v. 22, n. 2, p. 133, doi. 10.5414/TEP22133
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- Article
Allelic Variants of ARMC5 in Patients With Adrenal Incidentalomas and in Patients With Cushing's Syndrome Associated With Bilateral Adrenal Nodules.
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- Frontiers in Endocrinology, 2020, v. 11, p. 1, doi. 10.3389/fendo.2020.00036
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- Article
Computational Studies Applied to Flavonoids against Alzheimer's and Parkinson's Diseases.
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- Oxidative Medicine & Cellular Longevity, 2018, v. 2018, p. 1, doi. 10.1155/2018/7912765
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- Article
Impact of Glucocorticoid Receptor Gene Polymorphisms on the Metabolic Profile of Adult Patients with the Classical Form of 21-Hydroxylase Deficiency.
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- PLoS ONE, 2012, v. 7, n. 9, p. 1, doi. 10.1371/journal.pone.0044893
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- Article
A severe phenotype of Kennedy disease associated with a very large CAG repeat expansion.
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- 2018
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- Case Study
Novel Heterozygous Nonsense GLI2 Mutations in Patients with Hypopituitarism and Ectopic Posterior Pituitary Lobe without Holoprosencephaly.
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- Journal of Clinical Endocrinology & Metabolism, 2010, v. 95, n. 11, p. E384, doi. 10.1210/jc.2010-1050
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- Publication type:
- Article