Works matching DE "POLYCYSTIC kidney disease treatment"
Results: 169
Semaphorin 7A in circulating regulatory T cells is increased in autosomal-dominant polycystic kidney disease and decreases with tolvaptan treatment.
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- Clinical & Experimental Nephrology, 2018, v. 22, n. 4, p. 906, doi. 10.1007/s10157-018-1542-x
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- Article
Polyuria due to vasopressin V2 receptor antagonism is not associated with increased ureter diameter in ADPKD patients.
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- Clinical & Experimental Nephrology, 2017, v. 21, n. 3, p. 375, doi. 10.1007/s10157-016-1297-1
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- Article
The effect of tolvaptan on autosomal dominant polycystic kidney disease patients: a subgroup analysis of the Japanese patient subset from TEMPO 3:4 trial.
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- Clinical & Experimental Nephrology, 2015, v. 19, n. 5, p. 867, doi. 10.1007/s10157-015-1086-2
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- Article
Autosomal dominant polycystic kidney disease: recent advances in pathogenesis and potential therapies.
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- Clinical & Experimental Nephrology, 2013, v. 17, n. 3, p. 317, doi. 10.1007/s10157-012-0741-0
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- Article
Emphysematous cyst infection in autosomal dominant polycystic kidney disease.
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- 2012
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- Publication type:
- Letter
Successful steroid treatment of a patient with autosomal dominant polycystic kidney disease complicated by sarcoidosis.
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- Clinical & Experimental Nephrology, 2011, v. 15, n. 3, p. 442, doi. 10.1007/s10157-011-0412-6
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- Article
Hyperbaric oxygen therapy in a patient with autosomal dominant polycystic kidney disease with a perinephritic abscess.
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- Clinical & Experimental Nephrology, 2011, v. 15, n. 1, p. 141, doi. 10.1007/s10157-010-0348-2
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- Article
Autosomal Recessive Polycystic Kidney Disease Associated with Nephrogenic Rests: A Possible Consequence of Arrested Renal Maturation.
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- 2009
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- Case Study
Inheritance of polycystic kidney diesease in Persian cats.
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- Journal of Heredity, 1996, v. 87, n. 1, p. 1, doi. 10.1093/oxfordjournals.jhered.a022945
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- Publication type:
- Article
EP12.12: Two cases of prenatally diagnosed autosomal recessive polycystic kidney disease treated with intensive respiratory management.
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- Ultrasound in Obstetrics & Gynecology, 2017, v. 50, p. 304, doi. 10.1002/uog.18482
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- Article
Novel increasing dose regimen of tolvaptan for autosomal dominant polycystic kidney disease in patient with low tolerability.
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- 2018
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- Publication type:
- Letter to the Editor
Carbohydrate antigen 19–9 is significantly elevated in autosomal dominant polycystic kidney disease.
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- Nephrology, 2018, v. 23, n. 3, p. 210, doi. 10.1111/nep.12988
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- Publication type:
- Article
Fibroblast growth factor 23 and soluble Klotho in patients with autosomal dominant polycystic kidney disease.
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- Nephrology, 2017, v. 22, n. 11, p. 848, doi. 10.1111/nep.12862
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- Publication type:
- Article
KHA-CARI guideline recommendations for the diagnosis and management of autosomal dominant polycystic kidney disease.
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- Nephrology, 2016, v. 21, n. 8, p. 705, doi. 10.1111/nep.12658
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- Publication type:
- Article
Corrosion-like oesophagitis in a patient with polycystic kidneys and uraemia.
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- 2016
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- Publication type:
- Other
Identifying and integrating consumer perspectives in clinical practice guidelines on autosomal-dominant polycystic kidney disease.
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- Nephrology, 2016, v. 21, n. 2, p. 122, doi. 10.1111/nep.12579
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- Publication type:
- Article
NOS3 as a potential modifier of ADPKD phenotypic variability: Progress towards an answer.
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- 2014
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- Publication type:
- Editorial
Treatments to slow progression of autosomal dominant polycystic kidney disease: systematic review and meta-analysis of randomized trials.
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- Nephrology, 2014, v. 19, n. 4, p. 217, doi. 10.1111/nep.12211
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- Publication type:
- Article
Autosomal-dominant polycystic kidney disease.
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- Nephrology, 2007, v. 12, p. S52, doi. 10.1111/j.1440-1797.2006.00720.x
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- Publication type:
- Article
Treatment of Persistent Gross Hematuria with Tranexamic Acid in Autosomal Dominant Polycystic Kidney Disease.
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- Kidney & Blood Pressure Research, 2017, v. 42, n. 1, p. 156, doi. 10.1159/000474961
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- Publication type:
- Article
Autosomal Dominant Polycystic Kidney Disease: New Treatment Options and How to Test Their Efficacy.
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- Kidney & Blood Pressure Research, 2009, v. 32, n. 5, p. 380, doi. 10.1159/000254338
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- Article
Beneficial Effects of Combination Therapy with Olmesartan and Azelnidipine in Murine Polycystic Kidneys.
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- Kidney & Blood Pressure Research, 2009, v. 32, n. 4, p. 239, doi. 10.1159/000238821
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- Publication type:
- Article
Coping with missing data in phase III pivotal registration trials: Tolvaptan in subjects with kidney disease, a case study.
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- Pharmaceutical Statistics, 2017, v. 16, n. 4, p. 250, doi. 10.1002/pst.1808
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- Article
Quick Recertification Series.
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- JAAPA: Journal of the American Academy of Physician Assistants (Haymarket Media, Inc.), 2010, v. 23, n. 3, p. 68
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- Article
Candidate Risk Factors and Mechanisms for Tolvaptan-Induced Liver Injury Are Identified Using a Collaborative Cross Approach.
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- Toxicological Sciences, 2017, v. 156, n. 2, p. 438, doi. 10.1093/toxsci/kfw269
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- Article
Use of tolvaptan in autosomal polycystic kidney disease: A single center experience.
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- Anatolian Clinic Journal of Medical Sciences, 2023, v. 28, n. 3, p. 323, doi. 10.21673/anadoluklin.1343396
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- Article
Mumbai Doctors Remove 12.8kg 'Giant' Kidneys from a Man Suffering with ADPKD.
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- Indian Practitioner, 2020, v. 73, n. 3, p. 49
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- Article
Genome-wide methylation profiling of ADPKD identified epigenetically regulated genes associated with renal cyst development.
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- Human Genetics, 2014, v. 133, n. 3, p. 281, doi. 10.1007/s00439-013-1378-0
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- Article
Renal cyst growth is attenuated by a combination treatment of tolvaptan and pioglitazone, while pioglitazone treatment alone is not effective.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-58382-z
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- Article
Briefly Noted.
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- Seminars in Dialysis, 2011, v. 24, n. 5, p. 603, doi. 10.1111/j.1525-139X.2011.00963.x
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- Article
Complications of autosomal dominant polycystic kidney disease in hemodialysis patients.
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- 2000
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- Publication type:
- journal article
Surgical Cyst Decortication in Autosomal Dominant Polycystic Kidney Disease.
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- Journal of Endourology, 2013, v. 27, n. 5, p. 528, doi. 10.1089/end.2012.0529
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- Publication type:
- Article
Case Report Technical and Functional Implications of Hand-Assisted Laparoscopic Partial Nephrectomy in a Patient with Autosomal Dominant Polycystic Kidney Disease.
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- Journal of Endourology, 2007, v. 21, n. 6, p. 625, doi. 10.1089/end.2006.0347
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- Publication type:
- Article
ADPKD: Prototype of Cardiorenal Syndrome Type 4.
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- International Journal of Nephrology, 2011, p. 1, doi. 10.4061/2011/490795
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- Article
Comparison of Total Kidney Volume Quantification Methods in Autosomal Dominant Polycystic Disease for a Comprehensive Disease Assessment.
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- 2017
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- Publication type:
- journal article
Foreign Body Reaction to Dialysis Chatheter and Peritoneal Fluid Eosinophilia in a Child on Continuous Ambulatory Peritoneal Dialysis.
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- 2017
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- Publication type:
- journal article
Targeted Next Generation Sequencing Revealed Novel Variants in the PKD1 and PKD2 Genes of Iranian Patients with Autosomal Dominant Polycystic Kidney Disease.
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- Archives of Iranian Medicine (AIM), 2022, v. 25, n. 9, p. 600, doi. 10.34172/aim.2022.95
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- Publication type:
- Article
Inhibition of polycystin-L channel by the Chinese herb Sparganum stoloniferum Buch.-Ham.
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- Canadian Journal of Physiology & Pharmacology, 2006, v. 84, n. 8/9, p. 923, doi. 10.1139/Y06-040
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- Article
How worms' sex behavior can have a major impact on understanding human disease.
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- 2012
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- Publication type:
- Editorial
Review of Tolvaptan for Autosomal Dominant Polycystic Kidney Disease.
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- Pharmacotherapy, 2014, v. 34, n. 6, p. 605, doi. 10.1002/phar.1421
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- Publication type:
- Article
Saikosaponin-d inhibits proliferation by up-regulating autophagy via the CaMKKβ-AMPK-mTOR pathway in ADPKD cells.
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- Molecular & Cellular Biochemistry, 2018, v. 449, n. 1/2, p. 219, doi. 10.1007/s11010-018-3358-0
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- Publication type:
- Article
Relationship between intracranial aneurysms and the severity of autosomal dominant polycystic kidney disease.
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- Acta Neurochirurgica, 2017, v. 159, n. 12, p. 2325, doi. 10.1007/s00701-017-3316-8
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- Publication type:
- Article
Massive renal size is not a contraindication to a laparoscopic approach for bilateral native nephrectomies in autosomal dominant polycystic kidney disease ( ADPKD).
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- BJU International, 2015, v. 115, n. 5, p. 796, doi. 10.1111/bju.12821
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- Publication type:
- Article
Laparoscopic Bilateral Native Nephrectomies with Simultaneous Kidney Transplantation.
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- BJU International, 2012, v. 110, n. 11c, p. E1008, doi. 10.1111/j.1464-410X.2012.11386.x
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- Publication type:
- Article
Novel PKD1 and PKD2 mutations in Taiwanese patients with autosomal dominant polycystic kidney disease.
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- Journal of Human Genetics, 2013, v. 58, n. 11, p. 720, doi. 10.1038/jhg.2013.91
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- Publication type:
- Article
Management of nephrolithiasis in autosomal dominant polycystic kidney disease - A single center experience.
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- Urology Annals, 2012, v. 4, n. 1, p. 29, doi. 10.4103/0974-7796.91618
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- Publication type:
- Article
The Treatment of Autosomal Dominant Polycystic Kidney Disease.
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- Deutsches Ärzteblatt International, 2015, v. 112, n. 51/52, p. 884, doi. 10.3238/arztebl.2015.0884
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- Publication type:
- Article
Treatment prospects for autosomal-dominant polycystic kidney disease.
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- Kidney International, 2001, v. 59, n. 6, p. 2005, doi. 10.1046/j.1523-1755.2001.00716.x
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- Publication type:
- Article
Citrate therapy for polycystic kidney disease in rats.
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- Kidney International, 2000, v. 58, n. 5, p. 1859, doi. 10.1111/j.1523-1755.2000.00357.x
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- Publication type:
- Article
Novel calcium-sensing receptor cytoplasmic tail deletion mutation causing autosomal dominant hypocalcemia: molecular and clinical study.
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- European Journal of Endocrinology, 2016, v. 174, n. 4, p. K1, doi. 10.1530/EJE-15-1216
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- Publication type:
- Article