Kale G - Search Results

1

The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene.

Gempel K, Topaloglu H, Talim B, Schneiderat P, Schoser BG, Hans VH, Pálmafy B, Kale G, Tokatli A, Quinzii C, Hirano M, Naini A, DiMauro S, Prokisch H, Lochmüller H, Horvath R. Gempel K, et al. Among authors: kale g. Brain. 2007 Aug;130(Pt 8):2037-44. doi: 10.1093/brain/awm054. Epub 2007 Apr 5. Brain. 2007. PMID: 17412732 Free PMC article.

2

LARGE expression in different types of muscular dystrophies other than dystroglycanopathy.

Balci-Hayta B, Talim B, Kale G, Dincer P. Balci-Hayta B, et al. Among authors: kale g. BMC Neurol. 2018 Dec 15;18(1):207. doi: 10.1186/s12883-018-1207-0. BMC Neurol. 2018. PMID: 30553274 Free PMC article.

3

A novel form of recessive limb girdle muscular dystrophy with mental retardation and abnormal expression of alpha-dystroglycan.

Dinçer P, Balci B, Yuva Y, Talim B, Brockington M, Dinçel D, Torelli S, Brown S, Kale G, Haliloglu G, Gerçeker FO, Atalay RC, Yakicier C, Longman C, Muntoni F, Topaloglu H. Dinçer P, et al. Among authors: kale g. Neuromuscul Disord. 2003 Dec;13(10):771-8. doi: 10.1016/s0960-8966(03)00161-5. Neuromuscul Disord. 2003. PMID: 14678799

4

An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker-Warburg syndrome (WWS) caused by a mutation in the POMT1 gene.

Balci B, Uyanik G, Dincer P, Gross C, Willer T, Talim B, Haliloglu G, Kale G, Hehr U, Winkler J, Topaloğlu H. Balci B, et al. Among authors: kale g. Neuromuscul Disord. 2005 Apr;15(4):271-5. doi: 10.1016/j.nmd.2005.01.013. Neuromuscul Disord. 2005. PMID: 15792865

5

Clinical and histopathological study of merosin-deficient and merosin-positive congenital muscular dystrophy.

Talim B, Kale G, Topaloglu H, Akçören Z, Caglar M, Gögüş S, Elkay M. Talim B, et al. Among authors: kale g. Pediatr Dev Pathol. 2000 Mar-Apr;3(2):168-76. doi: 10.1007/s100240050021. Pediatr Dev Pathol. 2000. PMID: 10679036

6

Beta-sarcoglycan gene mutations in Turkey.

Balci B, Wilichowski E, Haliloğlu G, Talim B, Aurino S, Kremer E, Ebinger F, Senbil N, Anlar B, Kale G, Nigro V, Topaloğlu H, Bonnemann C, Dinçer P. Balci B, et al. Among authors: kale g. Acta Myol. 2004 Dec;23(3):154-8. Acta Myol. 2004. PMID: 15938573

7

Congenital muscular dystrophy (non-Fukuyama type) in Turkey: a clinical and pathological evaluation.

Topaloğlu H, Yalaz K, Renda Y, Kale G, Cağlar M, Göğüş S. Topaloğlu H, et al. Among authors: kale g. Brain Dev. 1989;11(5):341-4. doi: 10.1016/s0387-7604(89)80066-x. Brain Dev. 1989. PMID: 2817300

8

Common deletion of mitochondrial DNA in a 5-year-old girl with failure to thrive, ptosis, ophthalmoplegia and ragged-red fibers.

Seyrantepe V, Kale G, Topaloglu H, Alikasifoglu A, Ozgüc M. Seyrantepe V, et al. Among authors: kale g. Brain Dev. 1999 Sep;21(6):413-5. doi: 10.1016/s0387-7604(99)00035-2. Brain Dev. 1999. PMID: 10487476

9

Inflammatory milieu of muscle biopsies in juvenile dermatomyositis.

Sag E, Kale G, Haliloglu G, Bilginer Y, Akcoren Z, Orhan D, Gucer S, Topaloglu H, Ozen S, Talim B. Sag E, et al. Among authors: kale g. Rheumatol Int. 2021 Jan;41(1):77-85. doi: 10.1007/s00296-020-04735-w. Epub 2020 Oct 26. Rheumatol Int. 2021. PMID: 33106894

10

A reevaluation of the structures accepted to represent the postnatal gubernaculum.

Tanyel FC, Talim B, Kale G, Büyükpamukçu N. Tanyel FC, et al. Among authors: kale g. Urol Int. 2002;69(2):116-9. doi: 10.1159/000065559. Urol Int. 2002. PMID: 12187041

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

189 results

Search Page

Filters