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Impact of Chaos on MOSFET Thermal Stress and Lifetime.
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- Electronics (2079-9292), 2024, v. 13, n. 9, p. 1649, doi. 10.3390/electronics13091649
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- Article
Imprint of Mesoscale Eddies on Air-Sea Interaction in the Tropical Atlantic Ocean.
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- Remote Sensing, 2023, v. 15, n. 12, p. 3087, doi. 10.3390/rs15123087
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- Article
Subsurface Eddy Detection Optimized with Potential Vorticity from Models in the Arabian Sea.
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- Journal of Atmospheric & Oceanic Technology, 2023, v. 40, n. 6, p. 677, doi. 10.1175/JTECH-D-22-0121.1
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- Article
Internal tides off the Amazon shelf during two contrasted seasons: interactions with background circulation and SSH imprints.
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- Ocean Science, 2022, v. 18, n. 6, p. 1591, doi. 10.5194/os-18-1591-2022
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- Article
Genotype, Mortality, Morbidity, and Outcomes of 3β-Hydroxysteroid Dehydrogenase Deficiency in Algeria.
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- Frontiers in Endocrinology, 2022, v. 13, p. 1, doi. 10.3389/fendo.2022.867073
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- Article
Clinical, biochemical, and biomolecular aspects of congenital adrenal hyperplasia in a group of Cameroonian children and adolescents.
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- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 6, p. 777, doi. 10.1515/jpem-2021-0696
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- Article
Internal tides off the Amazon shelf during two contrasted seasons: Interactions with background circulation and SSH imprints.
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- Ocean Science Discussions, 2022, p. 1, doi. 10.5194/os-2021-114
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- Article
The Impact of Chemical-Mechanical Ex Situ Aging on PFSA Membranes for Fuel Cells.
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- Membranes, 2021, v. 11, n. 5, p. 366, doi. 10.3390/membranes11050366
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- Article
Intra-Annual Rossby Waves Destabilization as a Potential Driver of Low-Latitude Zonal Jets: Barotropic Dynamics.
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- Journal of Physical Oceanography, 2021, v. 51, n. 2, p. 365, doi. 10.1175/JPO-D-20-0180.1
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- Article
Carbon dioxide emissions from transport and anemia influence on under-five mortality in Benin.
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- Environmental Science & Pollution Research, 2020, v. 27, n. 32, p. 40277, doi. 10.1007/s11356-020-09800-2
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- Article
Diapycnal mixing of passive tracers by Kelvin–Helmholtz instabilities.
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- Journal of Fluid Mechanics, 2020, v. 900, p. 1, doi. 10.1017/jfm.2020.483
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- Article
Preoperative Topical Estrogen Treatment vs Placebo in 244 Children With Midshaft and Posterior Hypospadias: Results of a Prospective, Multicenter, Double-Blind, Randomized, Placebo-Controlled Trial.
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- Journal of Clinical Endocrinology & Metabolism, 2020, v. 105, n. 7, p. 2422, doi. 10.1210/clinem/dgaa231
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- Article
Preoperative Topical Estrogen Treatment vs Placebo in 244 Children With Midshaft and Posterior Hypospadias.
- Published in:
- 2020
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- Publication type:
- journal article
Effects of upwelling duration and phytoplankton growth regime on dissolved-oxygen levels in an idealized Iberian Peninsula upwelling system.
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- Nonlinear Processes in Geophysics, 2020, v. 27, n. 2, p. 277, doi. 10.5194/npg-27-277-2020
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- Article
Disorder of sex development with germ cell tumors: Which is uncovered first?
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- 2020
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- Publication type:
- journal article
Observational study of disorders of sex development in Yaounde, Cameroon.
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- Journal of Pediatric Endocrinology & Metabolism, 2020, v. 33, n. 3, p. 417, doi. 10.1515/jpem-2019-0458
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- Publication type:
- Article
Observed Tracer Fields Structuration by Middepth Zonal Jets in the Tropical Pacific.
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- Journal of Physical Oceanography, 2020, v. 50, n. 2, p. 281, doi. 10.1175/JPO-D-19-0132.1
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- Article
Hypopituitarism in Patients with Blepharophimosis and FOXL2 Mutations.
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- Hormone Research in Paediatrics, 2020, v. 93, n. 1, p. 30, doi. 10.1159/000507249
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- Article
Exposure to Glucocorticoids in the First Part of Fetal Life is Associated with Insulin Secretory Defect in Adult Humans.
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- 2019
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- Publication type:
- journal article
Reversion SAMD9 Mutations Modifying Phenotypic Expression of MIRAGE Syndrome and Allowing Inheritance in a Usually de novo Disorder.
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- Frontiers in Endocrinology, 2019, p. 1, doi. 10.3389/fendo.2019.00625
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- Article
Observations and Mechanisms for the Formation of Deep Equatorial and Tropical Circulation.
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- Earth & Space Science, 2019, v. 6, n. 3, p. 370, doi. 10.1029/2018EA000438
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- Article
Is interstitial 8p23 microdeletion responsible of 46,XY gonadal dysgenesis? One case report from birth to puberty.
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- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 3, p. N.PAG, doi. 10.1002/mgg3.558
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- Article
Intermediate and deep zonal jets properties in the tropical Pacific ocean from high-resolution in-situ data.
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- Geophysical Research Abstracts, 2019, v. 21, p. 1
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- Article
Physical and biogeochemical controls on dissolved oxygen in coastal upwelling systems: insights from a low complexity coupled model.
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- Geophysical Research Abstracts, 2019, v. 21, p. 1
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- Publication type:
- Article
Effects of upwelling duration and phytoplankton growth regime on dissolved oxygen levels in an idealized Iberian Peninsula upwelling system.
- Published in:
- Nonlinear Processes in Geophysics Discussions, 2019, p. 1, doi. 10.5194/npg-2019-47
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- Publication type:
- Article
Aberrant Splicing Is the Pathogenicity Mechanism of the p.Glu314Lys Variant in CYP11A1 Gene.
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- Frontiers in Endocrinology, 2018, p. 1, doi. 10.3389/fendo.2018.00491
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- Article
Triple-A syndrome: a wide spectrum of adrenal dysfunction.
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- European Journal of Endocrinology, 2018, v. 178, n. 3, p. 199, doi. 10.1530/EJE-17-0642
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- Article
Physical and biogeochemical controls on dissolved oxygen in coastal upwelling systems.
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- Geophysical Research Abstracts, 2018, v. 20, p. 3388
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- Publication type:
- Article
A novel disorder of sex development, characterized by progressive regression of testicular function and cystic leukoencephalopathy.
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- American Journal of Medical Genetics. Part A, 2017, v. 173, n. 3, p. 654, doi. 10.1002/ajmg.a.38093
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- Article
Prenatal diagnosis of steroid 21-hydroxylase-deficient congenital adrenal hyperplasia: Experience from a tertiary care centre in India.
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- Indian Journal of Medical Research, 2017, v. 145, n. 2, p. 194, doi. 10.4103/ijmr.IJMR_329_16
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- Article
Growth curves for congenital adrenal hyperplasia from a national retrospective cohort.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 12, p. 1379, doi. 10.1515/jpem-2016-0156
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- Article
P450 Oxidoreductase Deficiency: Loss of Activity Caused by Protein Instability From a Novel L374H Mutation.
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- 2016
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- Publication type:
- journal article
NNT mutations: a cause of primary adrenal insufficiency, oxidative stress and extra-adrenal defects.
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- European Journal of Endocrinology, 2016, v. 175, n. 1, p. 73, doi. 10.1530/EJE-16-0056
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- Article
Laparoscopic-assisted vaginal pull-through: A new approach for congenital adrenal hyperplasia patients with high urogenital sinus.
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- 2015
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- Publication type:
- journal article
Macroprolactinaemia: a biological diagnostic strategy from the study of 222 patients.
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- European Journal of Endocrinology, 2015, v. 172, n. 6, p. 687, doi. 10.1530/EJE-14-1073
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- Article
Inadequate Cortisol Response to the Tetracosactide (Synacthen®) Test in Non-Classic Congenital Adrenal Hyperplasia: An Exception to the Rule?
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- Hormone Research in Paediatrics, 2015, v. 83, n. 4, p. 262, doi. 10.1159/000369901
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- Article
The effect of patient, provider and financing regulations on the intensity of ambulatory physical therapy episodes: a multilevel analysis based on routinely available data.
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- BMC Health Services Research, 2015, v. 15, n. 1, p. 1, doi. 10.1186/s12913-015-0686-6
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- Article
Severe sex differentiation disorder in a boy with a 3.8 Mb 10q25.3-q26.12 microdeletion encompassing EMX2.
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- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 10, p. 2618, doi. 10.1002/ajmg.a.36662
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- Article
New management strategy of pregnancies at risk of congenital adrenal hyperplasia using fetal sex determination in maternal serum: French cohort of 258 cases (2002-2011)
- Published in:
- 2014
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- Publication type:
- Journal Article
A man with a DAX1/NR0B1 mutation, normal puberty, and an intact hypothalamic-pituitary-gonadal axis but deteriorating oligospermia during long-term follow-up.
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- European Journal of Endocrinology, 2013, v. 168, n. 4, p. K45, doi. 10.1530/EJE-12-1055
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- Publication type:
- Article
Healthy birth after testicular extraction of sperm and ICSI from an azoospermic man with mild androgen insensitivity syndrome caused by an androgen receptor partial loss-of-function mutation.
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- Clinical Endocrinology, 2012, v. 77, n. 4, p. 593, doi. 10.1111/j.1365-2265.2012.04402.x
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- Article
A Novel SRY Mutation Leads to Asymmetric SOX9 Activation and Is Responsible for Mixed 46,XY Gonadal Dysgenesis.
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- Hormone Research in Paediatrics, 2012, v. 78, n. 3, p. 188, doi. 10.1159/000336925
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- Publication type:
- Article
Congenital lipoid adrenal hyperplasia (a rare form of adrenal insufficiency and ambiguous genitalia) caused by a novel mutation of the steroidogenic acute regulatory protein gene.
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- European Journal of Pediatrics, 2012, v. 171, n. 5, p. 787, doi. 10.1007/s00431-011-1620-5
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- Article
Impaired puberty, fertility, and final stature in 45,X/46,XY mixed gonadal dysgenetic patients raised as boys.
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- European Journal of Endocrinology, 2012, v. 166, n. 4, p. 687, doi. 10.1530/EJE-11-0756
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- Publication type:
- Article
Simulating the dynamics and intensification of cyclonic Loop Current Frontal Eddies in the Gulf of Mexico.
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- Journal of Geophysical Research. Oceans, 2012, v. 117, n. C2, p. n/a, doi. 10.1029/2011JC007279
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- Article
Precocious puberty and unlicensed paediatric drugs for severe hyperparathyroidism.
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- Nephrology Dialysis Transplantation, 2009, v. 24, n. 8, p. 2595, doi. 10.1093/ndt/gfp211
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- Article
Clinical and molecular characterization of a cohort of 161 unrelated women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency and 330 family members.
- Published in:
- 2009
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- Publication type:
- journal article
Thermal Mass Correction for the Evaluation of Salinity.
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- Journal of Atmospheric & Oceanic Technology, 2009, v. 26, n. 3, p. 665, doi. 10.1175/2008JTECHO612.1
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- Publication type:
- Article
CBP/p300-interacting transactivator, with Glu/Asp-rich C-terminal domain, 2, and pre-B-cell leukemia transcription factor 1 in human adrenal development and disease.
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- 2009
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- Publication type:
- journal article
CYP21A2 gene mutation analysis in Moroccan patients with classic form of 21-hydroxylase deficiency: high regional prevalence of p.Q318X mutation and identification of a novel p.L353R mutation.
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- Clinical Chemistry & Laboratory Medicine, 2008, v. 46, n. 12, p. 1707, doi. 10.1515/CCLM.2008.339
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- Article