Bech-Hansen NT - Search Results

1

Evaluation of APOE ɛ2/ɛ3/ɛ4 Alleles in a Cohort of Individuals Affected by Developmental Topographical Disorientation.

Barclay SF, Potocki K, Burles F, Bech-Hansen NT, Iaria G. Barclay SF, et al. Among authors: bech hansen nt. J Alzheimers Dis Rep. 2021 Jul 19;5(1):565-570. doi: 10.3233/ADR-210304. eCollection 2021. J Alzheimers Dis Rep. 2021. PMID: 34514340 Free PMC article.

2

Familial aggregation in developmental topographical disorientation (DTD).

Barclay SF, Burles F, Potocki K, Rancourt KM, Nicolson ML, Bech-Hansen NT, Iaria G. Barclay SF, et al. Among authors: bech hansen nt. Cogn Neuropsychol. 2016 Oct-Dec;33(7-8):388-397. doi: 10.1080/02643294.2016.1262835. Epub 2016 Dec 6. Cogn Neuropsychol. 2016. PMID: 27923326

3

ROHHAD and Prader-Willi syndrome (PWS): clinical and genetic comparison.

Barclay SF, Rand CM, Nguyen L, Wilson RJA, Wevrick R, Gibson WT, Bech-Hansen NT, Weese-Mayer DE. Barclay SF, et al. Among authors: bech hansen nt. Orphanet J Rare Dis. 2018 Jul 20;13(1):124. doi: 10.1186/s13023-018-0860-0. Orphanet J Rare Dis. 2018. PMID: 30029683 Free PMC article.

4

Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation (ROHHAD): exome sequencing of trios, monozygotic twins and tumours.

Barclay SF, Rand CM, Borch LA, Nguyen L, Gray PA, Gibson WT, Wilson RJ, Gordon PM, Aung Z, Berry-Kravis EM, Ize-Ludlow D, Weese-Mayer DE, Bech-Hansen NT. Barclay SF, et al. Among authors: bech hansen nt. Orphanet J Rare Dis. 2015 Aug 25;10:103. doi: 10.1186/s13023-015-0314-x. Orphanet J Rare Dis. 2015. PMID: 26302956 Free PMC article.

5

Absence of mutations in HCRT, HCRTR1 and HCRTR2 in patients with ROHHAD.

Barclay SF, Rand CM, Gray PA, Gibson WT, Wilson RJ, Berry-Kravis EM, Ize-Ludlow D, Bech-Hansen NT, Weese-Mayer DE. Barclay SF, et al. Among authors: bech hansen nt. Respir Physiol Neurobiol. 2016 Jan 15;221:59-63. doi: 10.1016/j.resp.2015.11.002. Epub 2015 Nov 10. Respir Physiol Neurobiol. 2016. PMID: 26555080

6

Extended evaluation of serotonin transporter gene functional polymorphisms in subjects with post-stroke depression.

Ramasubbu R, Tobias R, Bech-Hansen NT. Ramasubbu R, et al. Can J Psychiatry. 2008 Mar;53(3):197-201. doi: 10.1177/070674370805300310. Can J Psychiatry. 2008. PMID: 18441666

7

Sudden infant death syndrome (SIDS) in African Americans: polymorphisms in the gene encoding the stress peptide pituitary adenylate cyclase-activating polypeptide (PACAP).

Cummings KJ, Klotz C, Liu WQ, Weese-Mayer DE, Marazita ML, Cooper ME, Berry-Kravis EM, Tobias R, Goldie C, Bech-Hansen NT, Wilson RJ. Cummings KJ, et al. Acta Paediatr. 2009 Mar;98(3):482-9. doi: 10.1111/j.1651-2227.2008.01131.x. Epub 2008 Dec 17. Acta Paediatr. 2009. PMID: 19120039

8

Analysis of PAC1 receptor gene variants in Caucasian and African American infants dying of sudden infant death syndrome.

Barrett KT, Rodikova E, Weese-Mayer DE, Rand CM, Marazita ML, Cooper ME, Berry-Kravis EM, Bech-Hansen NT, Wilson RJ. Barrett KT, et al. Acta Paediatr. 2013 Dec;102(12):e546-52. doi: 10.1111/apa.12405. Acta Paediatr. 2013. PMID: 23981011

9

Transgenic Expression of Cacna1f Rescues Vision and Retinal Morphology in a Mouse Model of Congenital Stationary Night Blindness 2A (CSNB2A).

Waldner DM, Ito K, Chen LL, Nguyen L, Chow RL, Lee A, Rancourt DE, Tremblay F, Stell WK, Bech-Hansen NT. Waldner DM, et al. Among authors: bech hansen nt. Transl Vis Sci Technol. 2020 Oct 14;9(11):19. doi: 10.1167/tvst.9.11.19. eCollection 2020 Oct. Transl Vis Sci Technol. 2020. PMID: 33117610 Free PMC article.

10

Cone dystrophy and ectopic synaptogenesis in a Cacna1f loss of function model of congenital stationary night blindness (CSNB2A).

Waldner DM, Giraldo Sierra NC, Bonfield S, Nguyen L, Dimopoulos IS, Sauvé Y, Stell WK, Bech-Hansen NT. Waldner DM, et al. Among authors: bech hansen nt. Channels (Austin). 2018 Jan 1;12(1):17-33. doi: 10.1080/19336950.2017.1401688. Epub 2018 Jan 2. Channels (Austin). 2018. PMID: 29179637 Free PMC article.

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