Meyer BF - Search Results

1

Autosomal recessive hereditary spastic paraplegia with thin corpus callosum among Saudis.

Wakil SM, Murad HN, Baz BM, Hagos ST, Al-Amr RA, Al-Yamani SA, Al-Wadaee SM, Meyer BF, Bohlega SA. Wakil SM, et al. Among authors: meyer bf. Neurosciences (Riyadh). 2012 Jan;17(1):48-52. Neurosciences (Riyadh). 2012. PMID: 22246010

2

Localization of the gene for a novel autosomal recessive neurodegenerative Huntington-like disorder to 4p15.3.

Kambouris M, Bohlega S, Al-Tahan A, Meyer BF. Kambouris M, et al. Among authors: meyer bf. Am J Hum Genet. 2000 Feb;66(2):445-52. doi: 10.1086/302744. Am J Hum Genet. 2000. PMID: 10677304 Free PMC article.

3

A novel form of autosomal recessive pure hereditary spastic paraplegia maps to chromosome 13q14.

Hodgkinson CA, Bohlega S, Abu-Amero SN, Cupler E, Kambouris M, Meyer BF, Bharucha VA. Hodgkinson CA, et al. Among authors: meyer bf. Neurology. 2002 Dec 24;59(12):1905-9. doi: 10.1212/01.wnl.0000036909.49629.21. Neurology. 2002. PMID: 12499481

4

Autosomal dominant hyaline body myopathy: clinical variability and pathologic findings.

Bohlega S, Lach B, Meyer BF, Al Said Y, Kambouris M, Al Homsi M, Cupler EJ. Bohlega S, et al. Among authors: meyer bf. Neurology. 2003 Dec 9;61(11):1519-23. doi: 10.1212/01.wnl.0000096022.09887.9d. Neurology. 2003. PMID: 14663035

5

Mutation of the slow myosin heavy chain rod domain underlies hyaline body myopathy.

Bohlega S, Abu-Amero SN, Wakil SM, Carroll P, Al-Amr R, Lach B, Al-Sayed Y, Cupler EJ, Meyer BF. Bohlega S, et al. Among authors: meyer bf. Neurology. 2004 May 11;62(9):1518-21. doi: 10.1212/01.wnl.0000123255.92062.37. Neurology. 2004. PMID: 15136674

6

The peroxisome proliferator-activated receptor-gamma2 P12A polymorphism and type 2 diabetes in an Arab population.

Wakil SM, Al-Rubeaan K, Alsmadi O, Imtiaz F, Carroll P, Rajab M, Al-Katari S, Al-Katari M, Meyer BF. Wakil SM, et al. Among authors: meyer bf. Diabetes Care. 2006 Jan;29(1):171-2. doi: 10.2337/diacare.29.1.171. Diabetes Care. 2006. PMID: 16373923 No abstract available.

7

Phenotypic variation and allelic heterogeneity in young patients with Papillon-Lefèvre syndrome.

Ullbro C, El-Samadi S, Boumah C, Al-Yousef N, Wakil S, Twetman S, Alfadley A, Thestrup-Pedersen K, Meyer B. Ullbro C, et al. Acta Derm Venereol. 2006;86(1):3-7. doi: 10.1080/00015550510011619. Acta Derm Venereol. 2006. PMID: 16585980 Free article.

8

Novel mutations underlying nephrogenic diabetes insipidus in Arab families.

Carroll P, Al-Mojalli H, Al-Abbad A, Al-Hassoun I, Al-Hamed M, Al-Amr R, Butt AI, Meyer BF. Carroll P, et al. Among authors: meyer bf. Genet Med. 2006 Jul;8(7):443-7. doi: 10.1097/01.gim.0000223554.46981.7a. Genet Med. 2006. PMID: 16845277 Free article.

9

Recessive cornea plana in the Kingdom of Saudi Arabia.

Khan AO, Aldahmesh M, Meyer B. Khan AO, et al. Ophthalmology. 2006 Oct;113(10):1773-8. doi: 10.1016/j.ophtha.2006.04.026. Ophthalmology. 2006. PMID: 17011957

10

Genetic study of Saudi diabetes (GSSD): significant association of the KCNJ11 E23K polymorphism with type 2 diabetes.

Alsmadi O, Al-Rubeaan K, Wakil SM, Imtiaz F, Mohamed G, Al-Saud H, Al-Saud NA, Aldaghri N, Mohammad S, Meyer BF. Alsmadi O, et al. Among authors: meyer bf. Diabetes Metab Res Rev. 2008 Feb;24(2):137-40. doi: 10.1002/dmrr.777. Diabetes Metab Res Rev. 2008. PMID: 17922473

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