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The origins of the universe: why is there something rather than nothing?
- Published in:
- Annals of the New York Academy of Sciences, 2015, v. 1361, n. 1, p. 1, doi. 10.1111/nyas.12859
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- Publication type:
- Article
Supravesical urinary diversion: A comparison between cutaneous ureterostomy and heal conduit.
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- Journal of Surgical Oncology, 1970, v. 2, n. 3, p. 291, doi. 10.1002/jso.2930020313
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- Publication type:
- Article
Metastatic renal adenocarcinoma to the ureteral stump in a hemophiliac.
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- Journal of Surgical Oncology, 1970, v. 2, n. 2, p. 107, doi. 10.1002/jso.2930020205
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- Publication type:
- Article
Performance of hand-held electrocardiogram devices to detect atrial fibrillation in a cardiology and geriatric ward setting.
- Published in:
- 2017
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- Publication type:
- Letter
'They deserve better': reflecting on 'Reflecting the "human nature" of IVF embryos'.
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- Journal of Law & the Biosciences, 2017, v. 4, n. 2, p. 397, doi. 10.1093/jlb/lsx013
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- Publication type:
- Article
P‐210: Late‐News Poster: Advances in Infrared and Projected Capacitive Touch Screens.
- Published in:
- SID Symposium Digest of Technical Papers, 2018, v. 49, n. 1, p. 1897, doi. 10.1002/sdtp.12472
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- Publication type:
- Article
P-203: Frequency Multiplexed Projected Capacitive Touch Screen.
- Published in:
- SID Symposium Digest of Technical Papers, 2017, v. 48, n. 1, p. 2043, doi. 10.1002/sdtp.12077
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- Publication type:
- Article
Early Recovery of Salmonella from Food Using a 6-Hour Non-selective Pre-enrichment and Reformulation of Tetrathionate Broth.
- Published in:
- Frontiers in Microbiology, 2016, v. 7, p. 1, doi. 10.3389/fmicb.2016.02103
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- Publication type:
- Article
Germ-line Genetic Engineering: A Critical Look at Magisterial Catholic Teaching.
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- Christian Bioethics: Non-ecumenical Studies in Medical Morality, 2012, v. 18, n. 2, p. 126, doi. 10.1093/cb/cbs016
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- Publication type:
- Article
Sin, Suffering, and the Need for the Theological Virtues.
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- Christian Bioethics: Non-ecumenical Studies in Medical Morality, 2006, v. 12, n. 2, p. 187, doi. 10.1093/13803600600805526
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- Publication type:
- Article
Further delineation of the congenital form of X-linked dyskeratosis congenita (Hoyeraal-Hreidarsson syndrome).
- Published in:
- 2003
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- Publication type:
- journal article
Comment by Albert David.
- Published in:
- Journal of Multi-Criteria Decision Analysis, 1999, v. 8, n. 1, p. 19, doi. 10.1002/(SICI)1099-1360(199901)8:1<19::AID-MCDA214>3.0.CO;2-V
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- Publication type:
- Article
Barber-Say Syndrome and Ablepharon-Macrostomia Syndrome: A Patient's View.
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- Molecular Syndromology, 2017, v. 8, n. 4, p. 172, doi. 10.1159/000472408
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- Publication type:
- Article
Travailler en mode middleground: collectifs créatifs et institutions intermédiaires.
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- Management international / International Management / Gestiòn Internacional, 2021, v. 25, p. 122, doi. 10.7202/1088142ar
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- Publication type:
- Article
Nosology of fetal hypokinesia sequence based on CNS abnormalities: is there an Aase-Smith syndrome?
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- Clinical Genetics, 1996, v. 50, n. 4, p. 251, doi. 10.1111/j.1399-0004.1996.tb02638.x
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- Publication type:
- Article
Modeling chemical accumulation in sediment of small waterbodies accounting for sediment transport and water-sediment exchange processes over long periods.
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- Environmental Toxicology & Chemistry, 2017, v. 36, n. 12, p. 3223, doi. 10.1002/etc.3921
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- Publication type:
- Article
Tobacco education in dentistry and dental hygiene.
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- Drug & Alcohol Review, 2009, v. 28, n. 5, p. 517, doi. 10.1111/j.1465-3362.2009.00108.x
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- Publication type:
- Article
Role of Preoperative Basal Calcitonin Levels in the Timing of Prophylactic Thyroidectomy in Patients With Germline RET Mutations.
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- World Journal of Surgery, 2014, v. 38, n. 3, p. 576, doi. 10.1007/s00268-013-2413-y
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- Publication type:
- Article
Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations.
- Published in:
- 2015
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- Publication type:
- journal article
Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis.
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- Orphanet Journal of Rare Diseases, 2011, v. 6, n. 1, p. 21, doi. 10.1186/1750-1172-6-21
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- Publication type:
- Article
A panel study on patients with dominant cerebellar ataxia highlights the frequency of channelopathies.
- Published in:
- 2017
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- Publication type:
- journal article
Colloquy.
- Published in:
- National Catholic Bioethics Quarterly, 2019, v. 19, n. 3, p. 343, doi. 10.5840/ncbq201919324
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- Publication type:
- Article
Editing Out the Embryo.
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- National Catholic Bioethics Quarterly, 2017, v. 17, n. 1, p. 83
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- Publication type:
- Article
Magisterial Teaching on Vital Conflicts.
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- National Catholic Bioethics Quarterly, 2014, v. 14, n. 1, p. 81
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- Publication type:
- Article
Technology for Awakening Hard-of-Hearing People During Fire Emergencies.
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- Audiology Today, 2017, v. 29, n. 6, p. 45
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- Publication type:
- Article
A head-to-head comparison of fast-SENC and feature tracking to LV long axis strain for assessment of myocardial deformation in chest pain patients.
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- BMC Medical Imaging, 2022, v. 22, n. 1, p. 1, doi. 10.1186/s12880-022-00886-3
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- Publication type:
- Article
Spectral Estimation of the Electrocardiogram.
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- Annals of the New York Academy of Sciences, 1990, v. 601, n. 1, p. 197, doi. 10.1111/j.1749-6632.1990.tb37301.x
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- Publication type:
- Article
First record of pigmentation disorder in the Fringe-lipped Bat Trachops cirrhosus (Spix, 1823) (Chiroptera: Phyllostomidae) from southeast Brazil.
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- Biodiversity Data Journal, 2019, p. 1, doi. 10.3897/BDJ.7.e38304
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- Publication type:
- Article
First record of predation of Nyctinomops laticaudatus (É. Geoffroy, 1805) by Chrotopterus auritus (Peters, 1856) (Mammalia: Chiroptera).
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- Biodiversity Data Journal, 2019, p. 1, doi. 10.3897/BDJ.7.e38303
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- Publication type:
- Article
Lyme arthritis in Western Europe: a multicentre retrospective study.
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- European Journal of Clinical Microbiology & Infectious Diseases, 2022, v. 41, n. 1, p. 21, doi. 10.1007/s10096-021-04334-y
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- Publication type:
- Article
Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities.
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- 2016
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- Publication type:
- journal article
Phenotypic Spectrum of Simpson–Golabi–Behmel Syndrome in a Series of 42 Cases With a Mutation in GPC3 and Review of the Literature.
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- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2013, v. 163C, n. 2, p. 92, doi. 10.1002/ajmg.c.31360
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- Article
Factors Associated With Clinical Improvement and the Disappearance of Calcifications After Ultrasound-Guided Percutaneous Lavage of Rotator Cuff Calcific Tendinopathy: A Post Hoc Analysis of a Randomized Controlled Trial.
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- American Journal of Sports Medicine, 2021, v. 49, n. 4, p. 883, doi. 10.1177/0363546521992359
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- Article
Cat eye syndrome: Clinical, cytogenetics and familial findings in a large cohort of 43 patients highlighting the importance of congenital heart disease and inherited cases.
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- American Journal of Medical Genetics. Part A, 2024, v. 194, n. 4, p. 1, doi. 10.1002/ajmg.a.63476
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- Article
Familial autosomal dominant severe ankyloglossia with tooth abnormalities.
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- American Journal of Medical Genetics. Part A, 2018, v. 176, n. 7, p. 1614, doi. 10.1002/ajmg.a.38690
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- Article
Large national series of patients with Xq28 duplication involving MECP2: Delineation of brain MRI abnormalities in 30 affected patients.
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- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 1, p. 116, doi. 10.1002/ajmg.a.37384
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- Publication type:
- Article
Phenotype-genotype correlations in 17 new patients with an Xp11.23p11.22 microduplication and review of the literature.
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- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 1, p. 111, doi. 10.1002/ajmg.a.36807
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- Article
Interstitial 22q13 deletions not involving SHANK3 gene: A new contiguous gene syndrome.
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- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 7, p. 1666, doi. 10.1002/ajmg.a.36513
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- Publication type:
- Article
Blepharophimosis, short humeri, developmental delay and hirschsprung disease: Expanding the phenotypic spectrum of MED12 mutations.
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- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 7, p. 1821, doi. 10.1002/ajmg.a.36539
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- Publication type:
- Article
Duplication of exon 2 of the GPC3 gene in a case of Simpson-Golabi-Behmel syndrome.
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- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 1, p. 282, doi. 10.1002/ajmg.a.36199
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- Publication type:
- Article
A new form of severe spondyloepimetaphyseal dysplasia: Clinical and radiological characterization.
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- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 10, p. 2645, doi. 10.1002/ajmg.a.36132
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- Publication type:
- Article
Exudative retinopathy, cerebral calcifications, duodenal atresia, preaxial polydactyly, micropenis, microcephaly and short stature: A new syndrome?
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- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 8, p. 1829, doi. 10.1002/ajmg.a.36021
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- Publication type:
- Article
Constitutional telomeric association (Y;7) in a patient with a female phenotype.
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- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 6, p. 1436, doi. 10.1002/ajmg.a.35889
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- Publication type:
- Article
Palmo-Plantar hyperkeratosis, intellectual disability, and spastic paraplegia in two maternal half brothers: Further evidence for an X-linked inheritance.
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- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 6, p. 1390, doi. 10.1002/ajmg.a.35871
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- Publication type:
- Article
Progressive polyepiphyseal dysplasia with arthropathy: A distinct disorder from idiopathic juvenile arthritis and pseudorheumatoid dysplasia?
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- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 7, p. 1754, doi. 10.1002/ajmg.a.35424
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- Publication type:
- Article
Probabilistic classification learning with corrective feedback is associated with in vivo striatal dopamine release in the ventral striatum, while learning without feedback is not.
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- Human Brain Mapping, 2014, v. 35, n. 10, p. 5106, doi. 10.1002/hbm.22536
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- Article
Mutations in STAMBP, encoding a deubiquitinating enzyme, cause microcephaly-capillary malformation syndrome.
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- Nature Genetics, 2013, v. 45, n. 5, p. 556, doi. 10.1038/ng.2602
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- Publication type:
- Article
Truncating mutations in the last exon of NOTCH2 cause a rare skeletal disorder with osteoporosis.
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- Nature Genetics, 2011, v. 43, n. 4, p. 306, doi. 10.1038/ng.778
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- Article
Germline mutations in WTX cause a sclerosing skeletal dysplasia but do not predispose to tumorigenesis.
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- Nature Genetics, 2009, v. 41, n. 1, p. 95, doi. 10.1038/ng.270
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- Article
Diabetes and oral disease: implications for health professionals.
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- Annals of the New York Academy of Sciences, 2012, v. 1255, n. 1, p. 1, doi. 10.1111/j.1749-6632.2011.06460.x
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- Publication type:
- Article