Found: 29
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A Cyclic Nucleotide-Gated Channel (CNGC16) in Pollen Is Critical for Stress Tolerance in Pollen Reproductive Development.
- Published in:
- Plant Physiology, 2013, v. 161, n. 2, p. 1010, doi. 10.1104/pp.112.206888
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- Article
Telehealth Applications in Head and Neck Oncology.
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- Journal of Speech-Language Pathology & Audiology, 2005, v. 29, n. 3, p. 125
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- Publication type:
- Article
Prospective functional outcomes in sequential population based cohorts of stage III/ IV oropharyngeal carcinoma patients treated with 3D conformal vs. intensity modulated radiotherapy.
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- Journal of Otolaryngology -- Head & Neck Surgery, 2015, v. 44, n. 1, p. 17, doi. 10.1186/s40463-015-0068-4
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- Publication type:
- Article
Oncologic and Voice Outcomes after Treatment of Early Glottic Cancer: Transoral Laser Microsurgery versus Radiotherapy.
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- Journal of Otolaryngology -- Head & Neck Surgery, 2012, v. 41, n. 6, p. 381, doi. 10.2310/7070.2012.00043
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- Publication type:
- Article
Functional Outcomes after Treatment of Advanced Oropharyngeal Carcinoma with Radiation or Chemoradiation.
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- Journal of Otolaryngology -- Head & Neck Surgery, 2012, v. 41, n. 2, p. 108, doi. 10.2310/7070.2011.110211
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- Publication type:
- Article
Selected functional outcomes in advanced oral cancer: Comparison of surgery alone versus surgery with postoperative radiotherapy.
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- Head & Neck, 2022, v. 44, n. 3, p. 710, doi. 10.1002/hed.26968
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- Publication type:
- Article
Damaging de novo missense variants in EEF1A2 lead to a developmental and degenerative epileptic‐dyskinetic encephalopathy.
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- Human Mutation, 2020, v. 41, n. 7, p. 1263, doi. 10.1002/humu.24015
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- Publication type:
- Article
Reanalysis and optimisation of bioinformatic pipelines is critical for mutation detection.
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- Human Mutation, 2019, v. 40, n. 4, p. 374, doi. 10.1002/humu.23699
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- Publication type:
- Article
Contribution of ultrarare variants in mTOR pathway genes to sporadic focal epilepsies.
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- Annals of Clinical & Translational Neurology, 2019, v. 6, n. 3, p. 475, doi. 10.1002/acn3.722
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- Article
Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathy.
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- EMBO Molecular Medicine, 2015, v. 7, n. 12, p. 1580, doi. 10.15252/emmm.201505323
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- Publication type:
- Article
The co‐occurrence of Wilson disease and X‐linked agammaglobulinemia in one family highlights the promising diagnostic potential of proteolytic analysis.
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- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 4, p. 1, doi. 10.1002/mgg3.1172
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- Publication type:
- Article
Longitudinal functional outcomes and late effects of radiation following treatment of nasopharyngeal carcinoma: secondary analysis of a prospective cohort study.
- Published in:
- Journal of Otolaryngology -- Head & Neck Surgery, 2022, v. 51, n. 1, p. 1, doi. 10.1186/s40463-022-00593-7
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- Publication type:
- Article
Severe speech impairment is a distinguishing feature of FOXP1‐related disorder.
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- Developmental Medicine & Child Neurology, 2021, v. 63, n. 12, p. 1417, doi. 10.1111/dmcn.14955
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- Article
BRAT1 encephalopathy: a recessive cause of epilepsy of infancy with migrating focal seizures.
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- 2020
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- Publication type:
- journal article
Intestinal Pathology in Patients With Pathogenic ACTG2 -Variant Visceral Myopathy: 16 Patients From 12 Families and Review of the Literature.
- Published in:
- Pediatric & Developmental Pathology, 2022, v. 25, n. 6, p. 581, doi. 10.1177/10935266221107449
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- Publication type:
- Article
Cyclic Nucleotide Gated Channels 7 and 8 Are Essential for Male Reproductive Fertility.
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- PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0055277
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- Article
100 Questions & Answers About Head and Neck Cancer.
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- 2010
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- Publication type:
- Book Review
Meeting the Challenges of Oral and Head and Neck Cancer: A Survivor's Guide.
- Published in:
- 2010
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- Publication type:
- Book Review
The Utility of Symptom Checklists in Long-Term Postlaryngectomy Follow-Up of Tracheoesophageal Speakers.
- Published in:
- Canadian Journal of Speech-Language Pathology & Audiology, 2009, v. 33, n. 4, p. 174
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- Publication type:
- Article
p.P1379S, a benign variant with reduced ATP7B protein level in Wilson Disease.
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- Journal of Inherited Metabolic Disease Reports, 2020, v. 54, n. 1, p. 32, doi. 10.1002/jmd2.12127
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- Publication type:
- Article
Calcium-dependent protein kinases regulate polarized tip growth in pollen tubes.
- Published in:
- Plant Journal, 2009, v. 59, n. 4, p. 528, doi. 10.1111/j.1365-313X.2009.03894.x
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- Publication type:
- Article
De novo FZR1 loss-of-function variants cause developmental and epileptic encephalopathies.
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- 2022
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- Publication type:
- journal article
CHD2 variants are a risk factor for photosensitivity in epilepsy.
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- Brain: A Journal of Neurology, 2015, v. 138, n. 5, p. 1198, doi. 10.1093/brain/awv052
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- Publication type:
- Article
FBXO28 causes developmental and epileptic encephalopathy with profound intellectual disability.
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- Epilepsia (Series 4), 2021, v. 62, n. 1, p. e13, doi. 10.1111/epi.16784
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- Publication type:
- Article
Hedgehog regulates angiogenesis of intersegmental vessels through the VEGF signaling pathway.
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- Developmental Dynamics, 2012, v. 241, n. 6, p. 1034, doi. 10.1002/dvdy.23795
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- Publication type:
- Article
ETS family protein ETV2 is required for initiation of the endothelial lineage but not the hematopoietic lineage in the Xenopus embryo.
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- Developmental Dynamics, 2010, v. 239, n. 4, p. 1178, doi. 10.1002/dvdy.22277
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- Publication type:
- Article
A population‐based cost‐effectiveness study of early genetic testing in severe epilepsies of infancy.
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- Epilepsia (Series 4), 2018, v. 59, n. 6, p. 1177, doi. 10.1111/epi.14087
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- Publication type:
- Article
Advancing epilepsy genetics in the genomic era.
- Published in:
- Genome Medicine, 2015, v. 7, n. 1, p. 1, doi. 10.1186/s13073-015-0214-7
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- Publication type:
- Article
Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathy.
- Published in:
- EMBO Molecular Medicine, 2017, v. 9, n. 12, p. 1764, doi. 10.15252/emmm.201708525
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- Publication type:
- Article