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Pulmonary arteriovenous malformations in hereditary haemorrhagic telangiectasia: Correlations between computed tomography findings and cerebral complications.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Obstetrical and neonatal complications in hereditary haemorrhagic telangiectasia: A retrospective study.
- Published in:
- BJOG: An International Journal of Obstetrics & Gynaecology, 2023, v. 130, n. 3, p. 303, doi. 10.1111/1471-0528.17303
- By:
- Publication type:
- Article
Intra-venous bevacizumab in hereditary hemorrhagic telangiectasia (HHT): A retrospective study of 46 patients.
- Published in:
- PLoS ONE, 2017, v. 12, n. 11, p. 1, doi. 10.1371/journal.pone.0188943
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- Publication type:
- Article
Safety of thalidomide and bevacizumab in patients with hereditary hemorrhagic telangiectasia.
- Published in:
- 2019
- By:
- Publication type:
- journal article
European Reference Network For Rare Vascular Diseases (VASCERN) Outcome Measures For Hereditary Haemorrhagic Telangiectasia (HHT).
- Published in:
- 2018
- By:
- Publication type:
- journal article
How to improve specific databases for clinical data in rare diseases? The example of hereditary haemorrhagic telangiectasia.
- Published in:
- Journal of Evaluation in Clinical Practice, 2012, v. 18, n. 3, p. 523, doi. 10.1111/j.1365-2753.2010.01627.x
- By:
- Publication type:
- Article
Living well with kidney disease by patient and care‐partner empowerment: Kidney health for everyone everywhere.
- Published in:
- Nephrology, 2021, v. 26, n. 3, p. 211, doi. 10.1111/nep.13829
- By:
- Publication type:
- Article
Functional analysis of endoglin mutations from hereditary hemorrhagic telangiectasia type 1 patients reveals different mechanisms for endoglin loss of function.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 4, p. 1142, doi. 10.1093/hmg/ddu531
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- Publication type:
- Article
A Spectral Principal Component Analysis-Based Framework for Composite Hard/Soft Tissue Fluorescence Image Investigation.
- Published in:
- Frontiers in Physiology, 2022, v. 13, p. 1, doi. 10.3389/fphys.2022.899626
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- Publication type:
- Article
LIVING WELL WITH KIDNEY DISEASE BY PATIENT AND CAREPARTNER EMPOWERMENT: KIDNEY HEALTH FOR EVERYONE EVERYWHERE.
- Published in:
- Brunei International Medical Journal (BIMJ), 2021, v. 17, p. 17
- By:
- Publication type:
- Article
Bevacizumab in Patients With Hereditary Hemorrhagic Telangiectasia and Severe Hepatic Vascular Malformations and High Cardiac Output.
- Published in:
- JAMA: Journal of the American Medical Association, 2012, v. 307, n. 9, p. 948, doi. 10.1001/jama.2012.250
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- Publication type:
- Article
Deletion of the Spata3 Gene Induces Sperm Alterations and In Vitro Hypofertility in Mice.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 4, p. 1959, doi. 10.3390/ijms22041959
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- Publication type:
- Article
The lack of Tex44 causes severe subfertility with flagellar abnormalities in male mice.
- Published in:
- Cellular & Molecular Biology Letters, 2024, v. 29, n. 1, p. 1, doi. 10.1186/s11658-024-00587-5
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- Publication type:
- Article
Response to Bevacizumab for the treatment of Rendu-Osler disease-A note of caution.
- Published in:
- Liver International, 2017, v. 37, n. 6, p. 928, doi. 10.1111/liv.13385
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- Publication type:
- Article
Hereditary hemorrhagic telangiectasia: to transplant or not to transplant?
- Published in:
- Liver International, 2016, v. 36, n. 12, p. 1741, doi. 10.1111/liv.13210
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- Publication type:
- Article
The Lung in Hereditary Hemorrhagic Telangiectasia.
- Published in:
- Respiration, 2017, v. 94, n. 4, p. 315, doi. 10.1159/000479632
- By:
- Publication type:
- Article
Pulmonary Vascular Manifestations of Hereditary Hemorrhagic Telangiectasia (Rendu-Osler Disease).
- Published in:
- Respiration, 2007, v. 74, n. 4, p. 361, doi. 10.1159/000103205
- By:
- Publication type:
- Article
Genetic variation in the functional ENG allele inherited from the non-affected parent associates with presence of pulmonary arteriovenous malformation in hereditary hemorrhagic telangiectasia 1 (HHT1) and may influence expression of PTPN14.
- Published in:
- Frontiers in Genetics, 2015, v. 6, p. 1, doi. 10.3389/fgene.2015.00067
- By:
- Publication type:
- Article
Effect of Bevacizumab Nasal Spray on Epistaxis Duration in Hereditary Hemorrhagic Telangectasia: A Randomized Clinical Trial.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Hereditary hemorrhagic telangiectasia: evidence for regional founder effects of ACVRL1 mutations in French and Italian patients.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 6, p. 742, doi. 10.1038/ejhg.2008.3
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- Publication type:
- Article
Living well with kidney disease by patient and care-partner empowerment: kidney health for everyone everywhere.
- Published in:
- Brazilian Journal of Medical & Biological Research, 2021, v. 54, n. 6, p. 1, doi. 10.1590/1414-431X202011098
- By:
- Publication type:
- Article
Living well with kidney disease by patient and care-partner empowerment: kidney health for everyone everywhere.
- Published in:
- Brazilian Journal of Medical & Biological Research, 2021, v. 54, n. 1, p. 1, doi. 10.1590/1414-431X202011098
- By:
- Publication type:
- Article
Logic Locking: A Survey of Proposed Methods and Evaluation Metrics.
- Published in:
- Journal of Electronic Testing, 2019, v. 35, n. 3, p. 273, doi. 10.1007/s10836-019-05800-4
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- Publication type:
- Article
Secure JTAG Implementation Using Schnorr Protocol.
- Published in:
- Journal of Electronic Testing, 2013, v. 29, n. 2, p. 193, doi. 10.1007/s10836-013-5369-9
- By:
- Publication type:
- Article
Living well with kidney disease by patient and care partner empowerment: kidney health for everyone everywhere.
- Published in:
- Nephrology Dialysis Transplantation, 2021, v. 36, n. 2, p. 197, doi. 10.1093/ndt/gfaa336
- By:
- Publication type:
- Article
SKG-Lock+: A Provably Secure Logic Locking SchemeCreating Significant Output Corruption.
- Published in:
- Electronics (2079-9292), 2022, v. 11, n. 23, p. 3906, doi. 10.3390/electronics11233906
- By:
- Publication type:
- Article
Hereditary hemorrhagic telangiectasia and health-related quality of life: a qualitative investigation.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Classical Ehlers‐Danlos syndrome with a propensity to arterial events: A new report on a French family with a COL1A1 p.(Arg312Cys) variant.
- Published in:
- Clinical Genetics, 2020, v. 97, n. 2, p. 357, doi. 10.1111/cge.13643
- By:
- Publication type:
- Article
Living Well with Kidney Disease by Patient and Care-Partner Empowerment: Kidney Health for Everyone Everywhere.
- Published in:
- 2021
- By:
- Publication type:
- editorial
Living Well with Kidney Disease by Patient and Care-Partner Empowerment: Kidney Health for Everyone Everywhere.
- Published in:
- Saudi Journal of Kidney Diseases & Transplantation, 2021, v. 32, n. 2, p. 289, doi. 10.4103/1319-2442.335439
- By:
- Publication type:
- Article
Living Well with Kidney Disease by Patient and Care-Partner Empowerment: Kidney Health for Everyone Everywhere.
- Published in:
- Indian Journal of Nephrology, 2021, v. 31, n. 2, p. 83, doi. 10.4103/ijn.IJN_59_21
- By:
- Publication type:
- Article
Efficacy and safety of intravenous bevacizumab on severe bleeding associated with hemorrhagic hereditary telangiectasia: A national, randomized multicenter trial.
- Published in:
- Journal of Internal Medicine, 2023, v. 294, n. 6, p. 761, doi. 10.1111/joim.13714
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- Publication type:
- Article
Living well with kidney disease by patient and care partner empowerment: kidney health for everyone everywhere.
- Published in:
- Transplant International, 2021, v. 34, n. 3, p. 391, doi. 10.1111/tri.13811
- By:
- Publication type:
- Article
Living Well With Kidney Disease by Patient and Care-Partner Empowerment: Kidney Health for Everyone Everywhere.
- Published in:
- 2021
- By:
- Publication type:
- Editorial
Living Well With Kidney Disease by Patient and Care-Partner Empowerment: Kidney Health for Everyone Everywhere.
- Published in:
- 2021
- By:
- Publication type:
- Editorial
Living well with kidney disease by patient and care-partner empowerment: Kidney health for everyone everywhere.
- Published in:
- Nefrologia, 2021, v. 41, n. 2, p. 95, doi. 10.1016/j.nefro.2020.12.001
- By:
- Publication type:
- Article
Hemorrhagic Hereditary Telangiectasia (Rendu-Osler Disease) and Infectious Diseases: An Underestimated Association.
- Published in:
- Clinical Infectious Diseases, 2007, v. 44, n. 6, p. 841, doi. 10.1086/511645
- By:
- Publication type:
- Article
Thirty Years of Research into Rendu-Osler-Weber Disease in France: Historical Demography, Population Genetics and Molecular Biology.
- Published in:
- Population (1634-2941), 2009, v. 64, n. 2, p. 273, doi. 10.3917/pope.902.0273
- By:
- Publication type:
- Article
X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-κB signaling.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 277
- By:
- Publication type:
- Article
Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 173, doi. 10.1038/76024
- By:
- Publication type:
- Article
Telomere elongation by hnRNP A1 and a derivative that interacts with telomeric repeats and telomerase.
- Published in:
- Nature Genetics, 1998, v. 19, n. 2, p. 199, doi. 10.1038/575
- By:
- Publication type:
- Article
Living Well with Kidney Disease by Patient and Care-Partner Empowerment: Kidney Health for Everyone Everywhere.
- Published in:
- Turkish Journal of Nephrology, 2021, v. 30, n. 2, p. 99, doi. 10.5152/turkjnephrol.2021.090320
- By:
- Publication type:
- Article
A new mutational hotspot in the SKI gene in the context of MFS/TAA molecular diagnosis.
- Published in:
- Human Genetics, 2020, v. 139, n. 4, p. 461, doi. 10.1007/s00439-019-02102-9
- By:
- Publication type:
- Article
Interleukin-7 receptorα (IL-7Rα) deficiency: cellular and molecular bases. Analysis of clinical, immunological, and molecular features in 16 novel patients.
- Published in:
- Immunological Reviews, 2005, v. 203, n. 1, p. 110, doi. 10.1111/j.0105-2896.2005.00234.x
- By:
- Publication type:
- Article
Comparative Evaluation of the Efficacy of Two Ectoparasiticides in Preventing the Acquisition of Borrelia burgdorferi by Ixodes scapularis and Ixodes ricinus : A Canine Ex Vivo Model.
- Published in:
- Microorganisms, 2024, v. 12, n. 1, p. 202, doi. 10.3390/microorganisms12010202
- By:
- Publication type:
- Article
Living well with kidney disease by patient and care‐partner empowerment: Kidney health for everyone everywhere.
- Published in:
- 2021
- By:
- Publication type:
- Editorial
ZEB2, a new candidate gene for asplenia.
- Published in:
- Orphanet Journal of Rare Diseases, 2014, v. 9, n. 1, p. 1, doi. 10.1186/1750-1172-9-2
- By:
- Publication type:
- Article
ZEB2, a new candidate gene for asplenia.
- Published in:
- 2014
- By:
- Publication type:
- case study
Correction to: Living Well with Kidney Disease by patient and care-partner empowerment: Kidney Health for Everyone Everywhere.
- Published in:
- 2021
- By:
- Publication type:
- Correction Notice
Living Well with Kidney Disease by patient and care-partner empowerment: Kidney Health for Everyone Everywhere.
- Published in:
- 2021
- By:
- Publication type:
- Editorial