Works matching DE "HYPOALDOSTERONISM"
Results: 116
Hyperkalaemic acidosis: blood pressure is the diagnostic clue.
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- Pediatric Nephrology, 2025, v. 40, n. 4, p. 967, doi. 10.1007/s00467-024-06590-4
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- Article
Decreased KLHL3 expression is involved in the pathogenesis of pseudohypoaldosteronism type II caused by cullin 3 mutation in vivo.
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- Clinical & Experimental Nephrology, 2018, v. 22, n. 6, p. 1251, doi. 10.1007/s10157-018-1593-z
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- Article
An infant with Cholestasis and Refractory Electrolyte Abnormalities.
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- Asian Journal of Pediatric Nephrology, 2022, v. 5, n. 1, p. 43, doi. 10.4103/ajpn.ajpn_36_21
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- Article
Pediatric Tubular and Inherited Disorders in Asia: Results of Preliminary Survey of the Asian Pediatric Nephrology Association (AsPNA) Tubular and Inherited Working Group.
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- Asian Journal of Pediatric Nephrology, 2022, v. 5, n. 1, p. 14, doi. 10.4103/ajpn.ajpn_2_22
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- Article
Hyperkalaemia in diabetes: a silent risk predicting poor outcomes.
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- Diabetic Medicine, 2018, v. 35, n. 8, p. 1049, doi. 10.1111/dme.13683
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- Article
Relative hypoaldosteronism in a patient with Wolcott-Rallison syndrome.
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- Diabetic Medicine, 2016, v. 33, n. 3, p. e13, doi. 10.1111/dme.12968
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- Article
Hyperreninemic hypoaldosteronism: a possible etiological factor of septic shock-induced acute renal failure.
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- 2003
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- journal article
Phylogenomics and sequence-structure-function relationships in the GmrSD family of Type IV restriction enzymes.
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- BMC Bioinformatics, 2015, v. 16, p. 1, doi. 10.1186/s12859-015-0773-z
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- Article
Pseudohypoaldosteronism type 1 and Liddle's syndrome mutations that affect the single-channel properties of the epithelial Na<sup>+</sup> channel.
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- Physiological Reports, 2015, v. 3, n. 11, p. 1, doi. 10.14814/phy2.12600
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- Article
A novel mutation in exon 9 of Cullin 3 gene contributes to aberrant splicing in pseudohypoaldosteronism type II.
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- FEBS Open Bio, 2018, v. 8, n. 3, p. 461, doi. 10.1002/2211-5463.12389
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- Article
Captopril-induced metabolic acidosis with hyperkalemia.
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- 1988
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- Publication type:
- journal article
Clinical Course and Follow-Up o Type 1 Pseudohypoaldosteronism.
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- Erciyes Medical Journal / Erciyes Tip Dergisi, 2018, v. 40, n. 3, p. 113, doi. 10.5152/etd.2018.0033
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- Article
WNK4 is the major WNK positively regulating NCC in the mouse kidney.
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- Bioscience Reports, 2014, v. 34, n. 3, p. 195, doi. 10.1042/BSR20140047
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- Article
Tiny Tim, diagnosed.
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- Contemporary OB/GYN, 2022, v. 67, n. 12, p. 3
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- Article
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities.
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- Nature, 2012, v. 482, n. 7383, p. 98, doi. 10.1038/nature10814
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- Article
Scholl solüsyonundaki sitrik aside bağlı gelişen Stevens-Johnson sendromu: Olgu sunumu
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- Asthma Allergy Immunology / Astim Allerji Immunoloji, 2014, v. 12, n. 2, p. 110
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- Article
Pseudohypoaldosteronism: report of three cases.
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- 2017
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- Case Study
Use of renin angiotensin system inhibitors in patients with chronic kidney disease.
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- Internal Medicine Journal, 2016, v. 46, n. 5, p. 626, doi. 10.1111/imj.13060
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- Article
A Japanese girl with aldosterone synthase deficiency requiring fludrocortisone until 10 years of age.
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- 2023
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- Case Study
Neonatal renal venous thrombosis followed by secondary pseudohypoaldosteronism.
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- Pediatrics International, 2012, v. 54, n. 6, p. 936, doi. 10.1111/j.1442-200X.2012.03617.x
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- Article
Pseudohypoaldosteronism in a Neonate Presenting as Life-Threatening Hyperkalemia.
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- Case Reports in Endocrinology, 2016, p. 1, doi. 10.1155/2016/6384697
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- Article
Autosomal Dominant Pseudohypoaldosteronism Type 1 in an Infant with Salt Wasting Crisis Associated with Urinary Tract Infection and Obstructive Uropathy.
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- Case Reports in Endocrinology, 2013, p. 1, doi. 10.1155/2013/524647
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- Article
Successful treatment of renal tubular acidosis and recurrent secondary struvite kidney stones with rituximab in a patient with primary Sjögren's syndrome.
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- Rheumatology, 2017, v. 56, n. 3, p. 498, doi. 10.1093/rheumatology/kew452
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- Article
An Unusual Initial Presentation of Sjögren's Syndrome: Severe Hypokalemic Paralysis Secondary to Distal Renal Tubular Acidosis.
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- 2013
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- Publication type:
- Case Study
An 11-month old with failure to thrive.
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- 2021
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- Publication type:
- Case Study
Tranzitorní pseudohypoaldosteronismus -- nefro-urologické „puzzle“.
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- Czecho-Slovak Pediatrics / Česko-Slovenská Pediatrie, 2014, v. 69, n. 1, p. 3
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- Article
A rare case of persistent hyperkalaemia.
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- 2021
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- Publication type:
- Case Study
An inducible transgenic mouse model for familial hypertension with hyperkalaemia (Gordon's syndrome or pseudohypoaldosteronism type II).
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- Clinical Science, 2013, v. 124, n. 12, p. 701, doi. 10.1042/CS20120430
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- Article
Clinical features and molecular basis of pseudohypoaldosteronism type 1.
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- Clinical Pediatric Endocrinology, 2017, v. 26, n. 3, p. 109, doi. 10.1297/cpe.26.109
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- Article
A novel mutation in the human mineralocorticoid receptor gene in a Japanese family with autosomal-dominant pseudohypoaldosteronism type 1.
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- 2016
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- Publication type:
- Case Study
A patient with pseudohypoaldosteronism type II complicated by congenital hypopituitarism carrying a KLHL3 mutation.
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- Clinical Pediatric Endocrinology, 2016, v. 25, n. 4, p. 127, doi. 10.1297/cpe.25.127
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- Article
A novel NR3C2 mutation in a Japanese patient with the renal form of pseudohypoaldosteronism type 1.
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- 2016
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- Publication type:
- Case Study
Two Japanese patients with the renal form of pseudohypoaldosteronism type 1 caused by mutations of NR3C2.
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- 2015
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- Publication type:
- Case Study
Liddle's-like syndrome associated with nephrotic syndrome secondary to membranous nephropathy: the first case report.
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- 2018
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- Publication type:
- journal article
TNF Lectin-Like Domain Restores Epithelial Sodium Channel Function in Frameshift Mutants Associated With Pseudohypoaldosteronism Type 1B.
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- Frontiers in Immunology, 2017, p. 1, doi. 10.3389/fimmu.2017.00601
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- Article
Identification of a Novel CYP11B2 Variant in a Family with Varying Degrees of Aldosterone Synthase Deficiency.
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- Journal of Clinical Research in Pediatric Endocrinology, 2024, v. 16, n. 1, p. 95, doi. 10.4274/jcrpe.galenos.2022.2022-3-4
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- Article
Nephrogenic Syndrome of Inappropriate Antidiuresis Mimicking Hyporeninemic Hypoaldosteronism: Case Report of Two Infants.
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- Journal of Clinical Research in Pediatric Endocrinology, 2023, v. 15, n. 2, p. 214, doi. 10.4274/jcrpe.galenos.2021.2021.0191
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- Article
Clinical Management in Systemic Type Pseudohypoaldosteronism Due to SCNN1B Variant and Literature Review.
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- Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 4, p. 446, doi. 10.4274/jcrpe.galenos.2020.2020.0107
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- Article
Clinical and Genetic Characteristics of Patients with Corticosterone Methyloxidase Deficiency Type 2: Novel Mutations in CYP11B2.
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- Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 2, p. 232, doi. 10.4274/jcrpe.galenos.2020.2019.0216
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- Article
Dermal and Ophthalmic Findings in Pseudohypoaldosteronism.
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- Journal of Clinical Research in Pediatric Endocrinology, 2015, v. 7, n. 2, p. 155, doi. 10.4274/jcrpe.1740
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- Article
CME-Labor 23.
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- Praxis (16618157), 2011, v. 100, n. 25, p. 1523, doi. 10.1024/1661-8157/a000746
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- Article
Regional anesthesia is safe and effective for lower limb orthopedic surgery in patient with renal tubular acidosis and hypokalemia.
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- 2018
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- Publication type:
- Case Study
NR3C2 microdeletions—an underrecognized cause of pseudohypoaldosteronism type 1A: a case report and literature review.
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- Laboratory Medicine, 2024, v. 5, n. 5, p. 640, doi. 10.1093/labmed/lmae005
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- Publication type:
- Article
Congenital primary adrenal insufficiency and selective aldosterone defects presenting as salt-wasting in infancy: a single center 10-year experience.
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- Italian Journal of Pediatrics, 2016, v. 42, p. 1, doi. 10.1186/s13052-016-0282-3
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- Publication type:
- Article
Hypokalaemic Periodic Paralysis with Renal Tubular Acidosis in Patients with Primary Sjögren's Syndrome Presenting as Quadriparesis and Recurrent Paraparesis.
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- Journal of the Indian Academy of Clinical Medicine, 2023, v. 24, n. 2, p. 155
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- Article
The clinical significance of aldosterone synthase deficiency: report of a novel mutation in the CYP11B2 gene.
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- BMC Endocrine Disorders, 2014, v. 14, n. 1, p. 7, doi. 10.1186/1472-6823-14-29
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- Publication type:
- Article
Severe hyperkalemia is rescued by low-potassium diet in renal βENaC-deficient mice.
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- Pflügers Archiv: European Journal of Physiology, 2017, v. 469, n. 10, p. 1387, doi. 10.1007/s00424-017-1990-2
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- Article
A unifying mechanism for WNK kinase regulation of sodium-chloride cotransporter.
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- Pflügers Archiv: European Journal of Physiology, 2015, v. 467, n. 11, p. 2235, doi. 10.1007/s00424-015-1708-2
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- Article
Parálisis periódica hipopotasémica asociada a acidosis tubular renal distal (tipo 1) e hipotiroidismo autoinmune.
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- Revista Mexicana de Endocrinología, Metabolismo y Nutrición, 2018, v. 5, n. 2, p. 75
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- Article
Multisystemic Severe Form Pseudohypoaldosteronism: Can Gastrostomy be Useful in the Management?
- Published in:
- 2016
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- Publication type:
- Case Study