Similar articles for PMID: 18756473

Year	Number of Results
1937	1
1967	1
1991	2
1992	2
1993	1
1994	1
1995	3
1996	3
1998	4
2000	5
2001	2
2002	4
2003	7
2004	15
2005	13
2006	29
2007	31
2008	46
2009	26
2010	9
2011	9
2012	6
2013	4
2014	1
2015	4
2018	2
2019	3
2021	2
2022	3
2023	1
2024	0

1

An idiopathic epilepsy syndrome linked to 3q13.3-q21 and missense mutations in the extracellular calcium sensing receptor gene.

Kapoor A, Satishchandra P, Ratnapriya R, Reddy R, Kadandale J, Shankar SK, Anand A. Kapoor A, et al. Ann Neurol. 2008 Aug;64(2):158-67. doi: 10.1002/ana.21428. Ann Neurol. 2008. PMID: 18756473

2

Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3.

Hedera P, Blair MA, Andermann E, Andermann F, D'Agostino D, Taylor KA, Chahine L, Pandolfo M, Bradford Y, Haines JL, Abou-Khalil B. Hedera P, et al. Neurology. 2007 Jun 12;68(24):2107-12. doi: 10.1212/01.wnl.0000261246.75977.89. Epub 2007 Mar 21. Neurology. 2007. PMID: 17377072

3

A novel locus for generalized epilepsy with febrile seizures plus in French families.

Baulac S, Gourfinkel-An I, Couarch P, Depienne C, Kaminska A, Dulac O, Baulac M, LeGuern E, Nabbout R. Baulac S, et al. Arch Neurol. 2008 Jul;65(7):943-51. doi: 10.1001/archneur.65.7.943. Arch Neurol. 2008. PMID: 18625863

4

Genetic analysis of a five generation Indian family with BPES: a novel missense mutation (p.Y215C).

Kumar A, Babu M, Raghunath A, Venkatesh CP. Kumar A, et al. Mol Vis. 2004 Jul 9;10:445-9. Mol Vis. 2004. PMID: 15257268 Free article.

5

Mutations in the calcium-sensing receptor: a new genetic risk factor for chronic pancreatitis?

Felderbauer P, Klein W, Bulut K, Ansorge N, Dekomien G, Werner I, Epplen JT, Schmitz F, Schmidt WE. Felderbauer P, et al. Scand J Gastroenterol. 2006 Mar;41(3):343-8. doi: 10.1080/00365520510024214. Scand J Gastroenterol. 2006. PMID: 16497624

6

Familial occipitotemporal lobe epilepsy and migraine with visual aura: linkage to chromosome 9q.

Deprez L, Peeters K, Van Paesschen W, Claeys KG, Claes LR, Suls A, Audenaert D, Van Dyck T, Goossens D, Del-Favero J, De Jonghe P. Deprez L, et al. Neurology. 2007 Jun 5;68(23):1995-2002. doi: 10.1212/01.wnl.0000262764.78511.17. Epub 2007 Apr 25. Neurology. 2007. PMID: 17460155

7

Absence of pathogenic calcium sensing receptor mutations in sporadic idiopathic hypoparathyroidism.

Sarin R, Tomar N, Ray D, Gupta N, Sharma YD, Goswami R. Sarin R, et al. Clin Endocrinol (Oxf). 2006 Sep;65(3):359-63. doi: 10.1111/j.1365-2265.2006.02604.x. Clin Endocrinol (Oxf). 2006. PMID: 16918956

8

Linkage analysis of idiopathic generalised epilepsy in families of probands with Juvenile Myoclonic Epilepsy and marker loci in the region of EPM 1 on chromosome 21 q: Unverricht-Lundborg disease and JME are not allelic variants.

Rees M, Curtis D, Parker K, Sundqvist A, Baralle D, Bespalova IN, Burmeister M, Chung E, Gardiner RM, Whitehouse WP. Rees M, et al. Neuropediatrics. 1994 Feb;25(1):20-5. doi: 10.1055/s-2008-1071576. Neuropediatrics. 1994. PMID: 8208346

9

A novel mutation of the calcium sensing receptor gene is associated with chronic pancreatitis in a family with heterozygous SPINK1 mutations.

Felderbauer P, Hoffmann P, Einwächter H, Bulut K, Ansorge N, Schmitz F, Schmidt WE. Felderbauer P, et al. BMC Gastroenterol. 2003 Nov 29;3:34. doi: 10.1186/1471-230X-3-34. BMC Gastroenterol. 2003. PMID: 14641934 Free PMC article.

10

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family.

Charlier C, Singh NA, Ryan SG, Lewis TB, Reus BE, Leach RJ, Leppert M. Charlier C, et al. Nat Genet. 1998 Jan;18(1):53-5. doi: 10.1038/ng0198-53. Nat Genet. 1998. PMID: 9425900

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