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Literature DB >> 31529157

Rare cause of severe hypertension in an adolescent boy presenting with short stature: Answers.

Zehra Yavas Abali¹, Gozde Yesil², Tarık Kirkgoz¹, Neslihan Cicek³, Harika Alpay³, Serap Turan¹, Abdullah Bereket¹, Tulay Guran⁴.

Abstract

Entities: Disease Species

Keywords: Familial hyperkalemic hypertension; Gordon syndrome; Low renin hypertension; Pseudohypoaldosteronism type 2

Year: 2019 PMID： 31529157 DOI： 10.1007/s00467-019-04352-1

Source DB: PubMed Journal: Pediatr Nephrol ISSN： 0931-041X Impact factor: 3.714

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13 in total

1. Familial hyperkalemic hypertension (Gordon syndrome): evidence for phenotypic variability in a study of 7 families.

Authors: S Disse-Nicodème; J M Achard; J Potier; M Delahousse; B Fiquet-Kempf; N Stern; A Blanchard; J C Guilbaud; P Niaudet; D Chauveau; B Dussol; Y Berland; P Dequiedt; J L Ader; M Paillard; J P Grünfeld; A Fournier; P Corvol; X Jeunemaitre
Journal: Adv Nephrol Necker Hosp Date: 2001

2. WNK kinases regulate thiazide-sensitive Na-Cl cotransport.

Authors: Chao-Ling Yang; Jordan Angell; Rose Mitchell; David H Ellison
Journal: J Clin Invest Date: 2003-04 Impact factor: 14.808

3. Chronic acidosis-induced growth retardation is mediated by proton-induced expression of Gs protein.

Authors: Ruth Goldberg; Ella Reshef-Bankai; Raymond Coleman; Jacob Green; Gila Maor
Journal: J Bone Miner Res Date: 2006-05 Impact factor: 6.741

4. Effect of chronic metabolic acidosis on the growth hormone/IGF-1 endocrine axis: new cause of growth hormone insensitivity in humans.

Authors: M Brüngger; H N Hulter; R Krapf
Journal: Kidney Int Date: 1997-01 Impact factor: 10.612

Review 5. Monogenic forms of hypertension.

Authors: Giacomo Domenico Simonetti; Markus G Mohaupt; Mario G Bianchetti
Journal: Eur J Pediatr Date: 2011-03-15 Impact factor: 3.183

Review 6. Diagnosis and treatment of low-renin hypertension.

Authors: Paolo Mulatero; Andrea Verhovez; Fulvio Morello; Franco Veglio
Journal: Clin Endocrinol (Oxf) Date: 2007-06-15 Impact factor: 3.478

7. Hypercalciuria in familial hyperkalemia and hypertension accompanies hyperkalemia and precedes hypertension: description of a large family with the Q565E WNK4 mutation.

Authors: Haim Mayan; Gabriel Munter; Miriam Shaharabany; Meir Mouallem; Rachel Pauzner; Eliezer J Holtzman; Zvi Farfel
Journal: J Clin Endocrinol Metab Date: 2004-08 Impact factor: 5.958

8. Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities.

Authors: Lynn M Boyden; Murim Choi; Keith A Choate; Carol J Nelson-Williams; Anita Farhi; Hakan R Toka; Irina R Tikhonova; Robert Bjornson; Shrikant M Mane; Giacomo Colussi; Marcel Lebel; Richard D Gordon; Ben A Semmekrot; Alain Poujol; Matti J Välimäki; Maria E De Ferrari; Sami A Sanjad; Michael Gutkin; Fiona E Karet; Joseph R Tucci; Jim R Stockigt; Kim M Keppler-Noreuil; Craig C Porter; Sudhir K Anand; Margo L Whiteford; Ira D Davis; Stephanie B Dewar; Alberto Bettinelli; Jeffrey J Fadrowski; Craig W Belsha; Tracy E Hunley; Raoul D Nelson; Howard Trachtman; Trevor R P Cole; Maury Pinsk; Detlef Bockenhauer; Mohan Shenoy; Priya Vaidyanathan; John W Foreman; Majid Rasoulpour; Farook Thameem; Hania Z Al-Shahrouri; Jai Radhakrishnan; Ali G Gharavi; Beatrice Goilav; Richard P Lifton
Journal: Nature Date: 2012-01-22 Impact factor: 49.962