Found: 19
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Laparoscopic enucleation of a renal cell carcinoma.
- Published in:
- 1994
- By:
- Publication type:
- journal article
Prevention of migraine during prodrome with naratriptan.
- Published in:
- Cephalalgia, 2000, v. 20, n. 2, p. 122, doi. 10.1046/j.1468-2982.2000.00030.x
- By:
- Publication type:
- Article
Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2011, v. 96, n. 9, p. E1457, doi. 10.1210/jc.2011-0170
- By:
- Publication type:
- Article
Novel Heterozygous Nonsense GLI2 Mutations in Patients with Hypopituitarism and Ectopic Posterior Pituitary Lobe without Holoprosencephaly.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2010, v. 95, n. 11, p. E384, doi. 10.1210/jc.2010-1050
- By:
- Publication type:
- Article
Growth Hormone (GH) Pharmacogenetics: Influence of GH Receptor Exon 3 Retention or Deletion on First-Year Growth Response and Final Height in Patients with Severe GH Deficiency.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 3, p. 1076, doi. 10.1210/jc.2005-2005
- By:
- Publication type:
- Article
The phenotypic spectrum associated with OTX2 mutations in humans.
- Published in:
- European Journal of Endocrinology, 2021, v. 185, n. 1, p. 121, doi. 10.1530/EJE-20-1453
- By:
- Publication type:
- Article
A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reduced GH1 expression in siblings with isolated GH deficiency (IGHD).
- Published in:
- European Journal of Endocrinology, 2016, v. 175, n. 2, p. K7, doi. 10.1530/EJE-15-0149
- By:
- Publication type:
- Article
Rederivation of a mutant line (prop 1) of zebrafish Danio rerio infected with Pseudoloma neurophilia using in vitro fertilization with eggs from pathogen‐free wild‐type (AB) females and sperm from prop 1 males.
- Published in:
- Journal of Fish Diseases, 2022, v. 45, n. 1, p. 35, doi. 10.1111/jfd.13529
- By:
- Publication type:
- Article
Il racconto della Shoah per il XXI secolo: Testi, testimonianze, film.
- Published in:
- Novecento.org, 2023, n. 19, p. 89
- By:
- Publication type:
- Article
Adult self‐reported childhood maltreatment types are associated with treatment satisfaction and alcohol relapse in patients with comorbid substance use and mental health disorders.
- Published in:
- American Journal on Addictions, 2024, v. 33, n. 5, p. 516, doi. 10.1111/ajad.13535
- By:
- Publication type:
- Article
A case of 'anaphylactic-like' reaction during LDL apheresis: a pathophysiological hypothesis on white wine containing metabisulphite.
- Published in:
- Transfusion Medicine, 2016, v. 26, n. 6, p. 460, doi. 10.1111/tme.12369
- By:
- Publication type:
- Article
Standardizing CRISPR-Cas13 knockdown technique to investigate the role of cdh2 gene in pituitary development through growth hormone expression and transcription factors.
- Published in:
- Frontiers in Endocrinology, 2024, p. 01, doi. 10.3389/fendo.2024.1466638
- By:
- Publication type:
- Article
Allelic Variants in Established Hypopituitarism Genes Expand Our Knowledge of the Phenotypic Spectrum.
- Published in:
- Genes, 2021, v. 12, n. 8, p. 1128, doi. 10.3390/genes12081128
- By:
- Publication type:
- Article
Corpus, Amore, Sessistenza: critica della ragione tattile e ontologia aptica a partire dalla “filosofia del corpo” di Jean-Luc Nancy.
- Published in:
- Teoria, 2021, v. 41, n. 2, p. 77, doi. 10.4454/teoria.v41i2.134
- By:
- Publication type:
- Article
Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes.
- Published in:
- Clinical Endocrinology, 2018, v. 88, n. 3, p. 425, doi. 10.1111/cen.13535
- By:
- Publication type:
- Article
Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations.
- Published in:
- Clinical Endocrinology, 2017, v. 87, n. 6, p. 725, doi. 10.1111/cen.13430
- By:
- Publication type:
- Article
HESX1 mutations in patients with congenital hypopituitarism: variable phenotypes with the same genotype.
- Published in:
- Clinical Endocrinology, 2016, v. 85, n. 3, p. 408, doi. 10.1111/cen.13067
- By:
- Publication type:
- Article
Relatively high frequency of non-synonymous GLI2 variants in patients with congenital hypopituitarism without holoprosencephaly.
- Published in:
- Clinical Endocrinology, 2013, v. 78, n. 4, p. 551, doi. 10.1111/cen.12044
- By:
- Publication type:
- Article
Acromegalic features in growth hormore (GH)-deficient patients after long-term GH therapy.
- Published in:
- Clinical Endocrinology, 2003, v. 59, n. 6, p. 788, doi. 10.1046/j.1365-2265.2003.01899.x
- By:
- Publication type:
- Article