Found: 153
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Changes in facial morphology after adenotonsillectomy in mouth-breathing children.
- Published in:
- International Journal of Paediatric Dentistry, 2011, v. 21, n. 5, p. 389, doi. 10.1111/j.1365-263X.2011.01117.x
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- Publication type:
- Article
In vivo regulation of p21 by the Kruppel-like factor 6 tumor-suppressor gene in mouse liver and human hepatocellular carcinoma.
- Published in:
- Oncogene, 2007, v. 26, n. 30, p. 4428, doi. 10.1038/sj.onc.1210223
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- Publication type:
- Article
Long-term and highly frequent monitor of 6.7 GHz methanol masers to statistically research periodic flux variations around high-mass protostars using the Hitachi 32-m.
- Published in:
- Proceedings of the International Astronomical Union, 2017, v. 13, n. S336, p. 45, doi. 10.1017/S1743921317011516
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- Publication type:
- Article
Astrometry of Galactic star-forming regions with VERA.
- Published in:
- Proceedings of the International Astronomical Union, 2007, v. 3, n. S248, p. 198, doi. 10.1017/S1743921308019042
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- Publication type:
- Article
Parallax measurement of the Galactic Mira variables with VERA.
- Published in:
- Proceedings of the International Astronomical Union, 2007, v. 3, n. S248, p. 206, doi. 10.1017/S174392130801908X
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- Publication type:
- Article
Population pharmacokinetic and pharmacodynamic analysis of a class IC antiarrhythmic, pilsicainide, in patients with cardiac arrhythmias.
- Published in:
- 2006
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- Publication type:
- Journal Article
Keratocyst of the buccal mucosa.
- Published in:
- 2018
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- Publication type:
- Case Study
Critical Role of IL-5 in Antigen-Induced Pulmonary Eosinophilia, but Not in Lymphocyte Activation.
- Published in:
- International Archives of Allergy & Immunology, 2003, v. 130, n. 3, p. 209, doi. 10.1159/000069513
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- Publication type:
- Article
Hot Carriers in CVD-Grown Graphene Device with a Top h-BN Layer.
- Published in:
- Journal of Nanomaterials, 2018, p. 1, doi. 10.1155/2018/5174103
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- Publication type:
- Article
Friction reducing properties of onion-like carbon based lubricant under high contact pressure.
- Published in:
- Tribology: Materials, Surfaces & Interfaces, 2012, v. 6, n. 3, p. 116, doi. 10.1179/1751584X12Y.0000000014
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- Publication type:
- Article
Effect of surfactant on tribological performance and tribochemistry of boric acid based colloidal lubricants.
- Published in:
- Tribology: Materials, Surfaces & Interfaces, 2012, v. 6, n. 3, p. 134, doi. 10.1179/1751584X12Y.0000000016
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- Publication type:
- Article
Effect of GDNF gene transfer into axotomized retinal ganglion cells using in vivo electroporation with a contact lens-type electrode.
- Published in:
- 2005
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- Publication type:
- Abstract
A genome-wide DNA methylation signature for SETD1B-related syndrome.
- Published in:
- Clinical Epigenetics, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13148-019-0749-3
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- Publication type:
- Article
Bilateral cerebellar cysts and cerebral white matter lesions with cortical dysgenesis: Expanding the phenotype of LAMB1 gene mutations.
- Published in:
- 2018
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- Publication type:
- Case Study
PRUNE1‐related disorder: Expanding the clinical spectrum.
- Published in:
- Clinical Genetics, 2018, v. 94, n. 3/4, p. 362, doi. 10.1111/cge.13385
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- Publication type:
- Article
Confirmation of SLC5A7‐related distal hereditary motor neuropathy 7 in a family outside Wales.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
A novel missense mutation affecting the same amino acid as the recurrent PACS1 mutation in Schuurs‐Hoeijmakers syndrome.
- Published in:
- 2018
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- Publication type:
- Letter to the Editor
Novel biallelic SZT2 mutations in 3 cases of early‐onset epileptic encephalopathy.
- Published in:
- Clinical Genetics, 2018, v. 93, n. 2, p. 266, doi. 10.1111/cge.13061
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- Publication type:
- Article
Identification of novel BCL11A variants in patients with epileptic encephalopathy: Expanding the phenotypic spectrum.
- Published in:
- Clinical Genetics, 2018, v. 93, n. 2, p. 368, doi. 10.1111/cge.13067
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- Publication type:
- Article
A case of atypical Kabuki syndrome arising from a novel missense variant in HNRNPK.
- Published in:
- Clinical Genetics, 2017, v. 92, n. 5, p. 554, doi. 10.1111/cge.13023
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- Publication type:
- Article
Response to Lefebvre et al.
- Published in:
- Clinical Genetics, 2017, v. 92, n. 5, p. 563, doi. 10.1111/cge.13011
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- Publication type:
- Article
Characterization of SPATA5-related encephalopathy in early childhood.
- Published in:
- Clinical Genetics, 2016, v. 90, n. 5, p. 437, doi. 10.1111/cge.12813
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- Publication type:
- Article
DNM1L-related encephalopathy in infancy with Leigh syndrome-like phenotype and suppression-burst.
- Published in:
- Clinical Genetics, 2016, v. 90, n. 5, p. 472, doi. 10.1111/cge.12805
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- Publication type:
- Article
Different X-linked KDM5C mutations in affected male siblings: is maternal reversion error involved?
- Published in:
- Clinical Genetics, 2016, v. 90, n. 3, p. 276, doi. 10.1111/cge.12767
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- Publication type:
- Article
Delineation of clinical features in Wiedemann--Steiner syndrome caused by KMT2A mutations.
- Published in:
- Clinical Genetics, 2016, v. 89, n. 1, p. 115, doi. 10.1111/cge.12586
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- Publication type:
- Article
Mutations in COG2 encoding a subunit of the conserved oligomeric golgi complex cause a congenital disorder of glycosylation.
- Published in:
- Clinical Genetics, 2015, v. 87, n. 5, p. 455, doi. 10.1111/cge.12417
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- Publication type:
- Article
De novo EEF1A2 mutations in patients with characteristic facial features, intellectual disability, autistic behaviors and epilepsy.
- Published in:
- Clinical Genetics, 2015, v. 87, n. 4, p. 356, doi. 10.1111/cge.12394
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- Publication type:
- Article
Atypical giant axonal neuropathy arising from a homozygous mutation by uniparental isodisomy.
- Published in:
- Clinical Genetics, 2015, v. 87, n. 4, p. 395, doi. 10.1111/cge.12455
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- Publication type:
- Article
Whole exome sequencing revealed biallelic IFT122 mutations in a family with CED1 and recurrent pregnancy loss.
- Published in:
- Clinical Genetics, 2014, v. 85, n. 6, p. 592, doi. 10.1111/cge.12215
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- Publication type:
- Article
Coffin-Siris syndrome is a SWI/ SNF complex disorder.
- Published in:
- Clinical Genetics, 2014, v. 85, n. 6, p. 548, doi. 10.1111/cge.12225
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- Publication type:
- Article
AKT3 and PIK3R2 mutations in two patients with megalencephaly-related syndromes: MCAP and MPPH.
- Published in:
- Clinical Genetics, 2014, v. 85, n. 4, p. 396, doi. 10.1111/cge.12188
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- Publication type:
- Article
Exome sequencing in a family with an X-linked lethal malformation syndrome: clinical consequences of hemizygous truncating OFD1 mutations in male patients.
- Published in:
- Clinical Genetics, 2013, v. 83, n. 2, p. 135, doi. 10.1111/j.1399-0004.2012.01885.x
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- Publication type:
- Article
FOXG1 mutations in Japanese patients with the congenital variant of Rett syndrome.
- Published in:
- Clinical Genetics, 2012, v. 82, n. 6, p. 569, doi. 10.1111/j.1399-0004.2011.01819.x
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- Publication type:
- Article
Association of genomic deletions in the STXBP1 gene with Ohtahara syndrome.
- Published in:
- Clinical Genetics, 2012, v. 81, n. 4, p. 399, doi. 10.1111/j.1399-0004.2011.01733.x
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- Publication type:
- Article
Paternal mosaicism of an STXBP1 mutation in OS.
- Published in:
- Clinical Genetics, 2011, v. 80, n. 5, p. 484, doi. 10.1111/j.1399-0004.2010.01575.x
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- Publication type:
- Article
Familial Simpson-Golabi-Behmel syndrome: studies of X-chromosome inactivation and clinical phenotypes in two female individuals with GPC3 mutations.
- Published in:
- Clinical Genetics, 2011, v. 80, n. 5, p. 466, doi. 10.1111/j.1399-0004.2010.01554.x
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- Publication type:
- Article
A novel homozygous mutation of DARS2 may cause a severe LBSL variant.
- Published in:
- Clinical Genetics, 2011, v. 80, n. 3, p. 293, doi. 10.1111/j.1399-0004.2011.01644.x
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- Publication type:
- Article
Exome sequencing of two patients in a family with atypical X-linked leukodystrophy.
- Published in:
- Clinical Genetics, 2011, v. 80, n. 2, p. 161, doi. 10.1111/j.1399-0004.2011.01721.x
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- Publication type:
- Article
Alu-related 5q35 microdeletions in Sotos syndrome.
- Published in:
- Clinical Genetics, 2008, v. 74, n. 4, p. 384, doi. 10.1111/j.1399-0004.2008.01032.x
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- Publication type:
- Article
CDKL5 disruption by t(X;18) in a girl with West syndrome.
- Published in:
- 2008
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- Publication type:
- Letter
A 4-Mb critical region for intrauterine growth retardation at 15q26.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 4, p. 340, doi. 10.1034/j.1399-0004.2002.620416.x
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- Publication type:
- Article
A 4q21-q22 deletion in a girl with severe growth retardation.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 3, p. 226, doi. 10.1034/j.1399-0004.2002.610311.x
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- Publication type:
- Article
Tectal neurons of the frog: Intracellular recording and labeling with cobalt electrodes.
- Published in:
- Journal of Comparative Neurology, 1986, v. 246, n. 2, p. 238, doi. 10.1002/cne.902460208
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- Publication type:
- Article
A rare cause of acute abdomen in a young female patient.
- Published in:
- Acta Gastro-Enterologica Belgica, 2021, v. 84, n. 2, p. 389, doi. 10.51821/84.2.389
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- Publication type:
- Article
Hepatolobectomy-induced depression of hepatic circulation and metabolism in the dog is counteracted by isoflurane, but not by halothane.
- Published in:
- 1999
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- Publication type:
- journal article
Association between Reduction of Muscle Mass and Faster Declines in Global Cognition among Older People: A 4-Year Prospective Cohort Study.
- Published in:
- Journal of Nutrition, Health & Aging, 2023, v. 27, n. 11, p. 932, doi. 10.1007/s12603-023-2007-9
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- Publication type:
- Article
Mice Lacking Osteopontin Show Normal Development and Bone Structure but Display Altered Osteoclast Formation In Vitro.
- Published in:
- Journal of Bone & Mineral Research, 1998, v. 13, n. 7, p. 1101, doi. 10.1359/jbmr.1998.13.7.1101
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- Publication type:
- Article
Study on Exercise Test Induced Sustained Ventricular Tachycardia.
- Published in:
- Japanese Journal of Clinical Sports Medicine / Nihon Rinsho Supotsu, 2005, v. 13, n. 2, p. 192
- By:
- Publication type:
- Article
Release of Non-Glycosylated Polymeric Immunoglobulin Receptor Protein.
- Published in:
- Scandinavian Journal of Immunology, 2003, v. 58, n. 4, p. 471, doi. 10.1046/j.1365-3083.2003.01325.x
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- Publication type:
- Article
Ontogeny of the Murine Ig Joining Chain Gene and Protein.
- Published in:
- Scandinavian Journal of Immunology, 2001, v. 54, n. 6, p. 613, doi. 10.1046/j.1365-3083.2001.01016.x
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- Publication type:
- Article