Loesch D - Search Results

1

Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation.

Tassone F, Protic D, Allen EG, Archibald AD, Baud A, Brown TW, Budimirovic DB, Cohen J, Dufour B, Eiges R, Elvassore N, Gabis LV, Grudzien SJ, Hall DA, Hessl D, Hogan A, Hunter JE, Jin P, Jiraanont P, Klusek J, Kooy RF, Kraan CM, Laterza C, Lee A, Lipworth K, Losh M, Loesch D, Lozano R, Mailick MR, Manolopoulos A, Martinez-Cerdeno V, McLennan Y, Miller RM, Montanaro FAM, Mosconi MW, Potter SN, Raspa M, Rivera SM, Shelly K, Todd PK, Tutak K, Wang JY, Wheeler A, Winarni TI, Zafarullah M, Hagerman RJ. Tassone F, et al. Among authors: loesch d. Cells. 2023 Sep 21;12(18):2330. doi: 10.3390/cells12182330. Cells. 2023. PMID: 37759552 Free PMC article. Review.

2

Fragile X syndrome: do professionals know about it?

Cohen J, Loesch DZ. Cohen J, et al. Among authors: loesch dz. Med J Aust. 1999 Jun 21;170(12):624. doi: 10.5694/j.1326-5377.1999.tb127927.x. Med J Aust. 1999. PMID: 10416440 No abstract available.

3

Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA.

Tassone F, Hagerman RJ, Loesch DZ, Lachiewicz A, Taylor AK, Hagerman PJ. Tassone F, et al. Among authors: loesch dz. Am J Med Genet. 2000 Sep 18;94(3):232-6. doi: 10.1002/1096-8628(20000918)94:3<232::aid-ajmg9>3.0.co;2-h. Am J Med Genet. 2000. PMID: 10995510

4

Melatonin profiles and sleep characteristics in boys with fragile X syndrome: a preliminary study.

Gould EL, Loesch DZ, Martin MJ, Hagerman RJ, Armstrong SM, Huggins RM. Gould EL, et al. Among authors: loesch dz. Am J Med Genet. 2000 Dec 11;95(4):307-15. Am J Med Genet. 2000. PMID: 11186882

5

Effect of the deficits of fragile X mental retardation protein on cognitive status of fragile x males and females assessed by robust pedigree analysis.

Loesch DZ, Huggins RM, Bui QM, Epstein JL, Taylor AK, Hagerman RJ. Loesch DZ, et al. J Dev Behav Pediatr. 2002 Dec;23(6):416-23. doi: 10.1097/00004703-200212000-00004. J Dev Behav Pediatr. 2002. PMID: 12476071

6

Relationship of deficits of FMR1 gene specific protein with physical phenotype of fragile X males and females in pedigrees: a new perspective.

Loesch DZ, Huggins RM, Bui QM, Taylor AK, Hagerman RJ. Loesch DZ, et al. Am J Med Genet A. 2003 Apr 15;118A(2):127-34. doi: 10.1002/ajmg.a.10099. Am J Med Genet A. 2003. PMID: 12655493

7

Effect of fragile X status categories and FMRP deficits on cognitive profiles estimated by robust pedigree analysis.

Loesch DZ, Huggins RM, Bui QM, Taylor AK, Pratt C, Epstein J, Hagerman RJ. Loesch DZ, et al. Am J Med Genet A. 2003 Sep 15;122A(1):13-23. doi: 10.1002/ajmg.a.20214. Am J Med Genet A. 2003. PMID: 12949966

8

Effect of the fragile X status categories and the fragile X mental retardation protein levels on executive functioning in males and females with fragile X.

Loesch DZ, Bui QM, Grigsby J, Butler E, Epstein J, Huggins RM, Taylor AK, Hagerman RJ. Loesch DZ, et al. Neuropsychology. 2003 Oct;17(4):646-657. doi: 10.1037/0894-4105.17.4.646. Neuropsychology. 2003. PMID: 14599277

9

Phenotypic variation and FMRP levels in fragile X.

Loesch DZ, Huggins RM, Hagerman RJ. Loesch DZ, et al. Ment Retard Dev Disabil Res Rev. 2004;10(1):31-41. doi: 10.1002/mrdd.20006. Ment Retard Dev Disabil Res Rev. 2004. PMID: 14994286 Review.

10

Evidence for, and a spectrum of, neurological involvement in carriers of the fragile X pre-mutation: FXTAS and beyond.

Loesch DZ, Churchyard A, Brotchie P, Marot M, Tassone F. Loesch DZ, et al. Clin Genet. 2005 May;67(5):412-7. doi: 10.1111/j.1399-0004.2005.00425.x. Clin Genet. 2005. PMID: 15811008

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