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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1984 1
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2001 2
2004 1
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2007 2
2009 1
2011 2
2012 1
2013 3
2014 1
2015 2
2016 1
2017 2
2018 4
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2020 6
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2023 7
2024 2

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44 results

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Page 1
Low-Renin Hypertension.
Athimulam S, Lazik N, Bancos I. Athimulam S, et al. Endocrinol Metab Clin North Am. 2019 Dec;48(4):701-715. doi: 10.1016/j.ecl.2019.08.003. Epub 2019 Sep 25. Endocrinol Metab Clin North Am. 2019. PMID: 31655771 Review.
Monogenic Etiology of Hypertension.
Singh V, Van Why SK. Singh V, et al. Med Clin North Am. 2024 Jan;108(1):157-172. doi: 10.1016/j.mcna.2023.06.005. Epub 2023 Jul 27. Med Clin North Am. 2024. PMID: 37951648 Review.
Gordon Syndrome: a continuing story.
O'Shaughnessy KM. O'Shaughnessy KM. Pediatr Nephrol. 2015 Nov;30(11):1903-8. doi: 10.1007/s00467-014-2956-7. Epub 2014 Dec 11. Pediatr Nephrol. 2015. PMID: 25503323 Review.
Gordon Syndrome (GS) is a rare familial hypertension syndrome with a characteristic hyperkalaemia which distinguishes it from other syndromic forms of hypertension that typically cause hypokalaemia. ...
Gordon Syndrome (GS) is a rare familial hypertension syndrome with a characteristic hyperkalaemia which distinguishes it from …
11Beta-hydroxylase deficiency and other syndromes of mineralocorticoid excess as a rare cause of endocrine hypertension.
Melcescu E, Phillips J, Moll G, Subauste JS, Koch CA. Melcescu E, et al. Horm Metab Res. 2012 Nov;44(12):867-78. doi: 10.1055/s-0032-1321851. Epub 2012 Aug 29. Horm Metab Res. 2012. PMID: 22932914 Review.
Apart from primary aldosteronism, mineralocorticoid excess can be caused by congenital adrenal hyperplasia (CAH) due to mutations of the 11beta-hydroxylase and 17alpha-hydroxylase genes, by inactivating mutations of the glucocorticoid receptor gene (Chrousos syndrome), endogenous …
Apart from primary aldosteronism, mineralocorticoid excess can be caused by congenital adrenal hyperplasia (CAH) due to mutations of the 11b …
Familial Gordon syndrome associated with a PIEZO2 mutation.
Alisch F, Weichert A, Kalache K, Paradiso V, Longardt AC, Dame C, Hoffmann K, Horn D. Alisch F, et al. Am J Med Genet A. 2017 Jan;173(1):254-259. doi: 10.1002/ajmg.a.37997. Epub 2016 Oct 7. Am J Med Genet A. 2017. PMID: 27714920 Review.
Gordon syndrome or distal arthrogryposis type 3 is a rare autosomal dominant disorder characterized by contractures of upper and lower limbs. ...Our analysis indicated that mild delay in psychomotor development and intellectual disability could be part of the phenot …
Gordon syndrome or distal arthrogryposis type 3 is a rare autosomal dominant disorder characterized by contractures of upper a …
Molecular insights from dysregulation of the thiazide-sensitive WNK/SPAK/NCC pathway in the kidney: Gordon syndrome and thiazide-induced hyponatraemia.
Glover M, O'Shaughnessy KM. Glover M, et al. Clin Exp Pharmacol Physiol. 2013 Dec;40(12):876-84. doi: 10.1111/1440-1681.12115. Clin Exp Pharmacol Physiol. 2013. PMID: 23683032 Review.
Mendelian syndromes of altered blood pressure demonstrate the importance of the distal nephron in this process and of the thiazide-sensitive pathway in particular. Gordon syndrome (GS), the phenotypic inverse of the salt-wasting Gitelman syndrome, is a condition of …
Mendelian syndromes of altered blood pressure demonstrate the importance of the distal nephron in this process and of the thiazide-sensitive …
A Spanish Family with Gordon Syndrome Due to a Variant in the Acidic Motif of WNK1.
Peces R, Peces C, Espinosa L, Mena R, Blanco C, Tenorio-Castaño J, Lapunzina P, Nevado J. Peces R, et al. Genes (Basel). 2023 Sep 27;14(10):1878. doi: 10.3390/genes14101878. Genes (Basel). 2023. PMID: 37895227 Free PMC article.
(1) Background: Gordon syndrome (GS) or familial hyperkalemic hypertension is caused by pathogenic variants in the genes WNK1, WNK4, KLHL3, and CUL3. ...
(1) Background: Gordon syndrome (GS) or familial hyperkalemic hypertension is caused by pathogenic variants in the genes WNK1, …
Gordon syndrome: literature review and a report of two cases.
Botha SJ, Bütow KW. Botha SJ, et al. Cleft Palate Craniofac J. 2015 Jan;52(1):e18-22. doi: 10.1597/13-075. Cleft Palate Craniofac J. 2015. PMID: 24878349 Review.
The aim of this article is to publish a literature review and report on two new cases of Gordon syndrome (GS), a rare syndrome documented to have an autosomal dominant inheritance pattern or to occur sporadically; it is characterized by camptodactyly, cleft palate, …
The aim of this article is to publish a literature review and report on two new cases of Gordon syndrome (GS), a rare syndrome …
Associated syndromes in patients with Pierre Robin Sequence.
Karempelis P, Hagen M, Morrell N, Roby BB. Karempelis P, et al. Int J Pediatr Otorhinolaryngol. 2020 Apr;131:109842. doi: 10.1016/j.ijporl.2019.109842. Epub 2019 Dec 30. Int J Pediatr Otorhinolaryngol. 2020. PMID: 31927149
Additionally, 3 patients had central hypoventilation syndrome, 3 patients had Duane syndrome, 2 patients had Cornelia de Lange syndrome, 2 patients had Emanuel syndrome, 2 patients had Gordon syndrome, 2 patients had Mobius syndrome, 2 patients had Nager syndrome. . …
Additionally, 3 patients had central hypoventilation syndrome, 3 patients had Duane syndrome, 2 patients had Cornelia de Lange syndrome, 2 p …
44 results