Salih M - Search Results

1

Disorders of gonadal development: a broad clinical, cytogenetic and histopathologic spectrum.

Siklar Z, Berberoğlu M, Adiyaman P, Salih M, Tükün A, Cetinkaya E, Aycan Z, Evliyaoğlu O, Ergur AT, Oçal G. Siklar Z, et al. Among authors: salih m. Pediatr Endocrinol Rev. 2007 Mar;4(3):210-7. Pediatr Endocrinol Rev. 2007. PMID: 17551482

2

The clinical, histologic, and genotypic spectrum of SEPN1-related myopathy: A case series.

Villar-Quiles RN, von der Hagen M, Métay C, Gonzalez V, Donkervoort S, Bertini E, Castiglioni C, Chaigne D, Colomer J, Cuadrado ML, de Visser M, Desguerre I, Eymard B, Goemans N, Kaindl A, Lagrue E, Lütschg J, Malfatti E, Mayer M, Merlini L, Orlikowski D, Reuner U, Salih MA, Schlotter-Weigel B, Stoetter M, Straub V, Topaloglu H, Urtizberea JA, van der Kooi A, Wilichowski E, Romero NB, Fardeau M, Bönnemann CG, Estournet B, Richard P, Quijano-Roy S, Schara U, Ferreiro A. Villar-Quiles RN, et al. Among authors: salih ma. Neurology. 2020 Sep 15;95(11):e1512-e1527. doi: 10.1212/WNL.0000000000010327. Epub 2020 Aug 13. Neurology. 2020. PMID: 32796131 Free PMC article.

3

Pseudoxanthoma elasticum: a rare cause of hypertension in children.

Ekim M, Tümer N, Atmaca L, Anadolu R, Salih M, Dönmez O, Ozkaya N. Ekim M, et al. Among authors: salih m. Pediatr Nephrol. 1998 Apr;12(3):183-5. doi: 10.1007/s004670050432. Pediatr Nephrol. 1998. PMID: 9630033

4

Diagnostic approach to prostate cancer using total prostate specific antigen-based parameters together.

Serdar MA, Oguz O, Olgun A, Seçkin B, Ilgan S, Hasimi A, Salih M, Peker F, Kutluay T. Serdar MA, et al. Among authors: salih m. Ann Clin Lab Sci. 2002 Winter;32(1):22-30. Ann Clin Lab Sci. 2002. PMID: 11848613

5

Clinical and molecular genetic findings in COLQ-mutant congenital myasthenic syndromes.

Mihaylova V, Müller JS, Vilchez JJ, Salih MA, Kabiraj MM, D'Amico A, Bertini E, Wölfle J, Schreiner F, Kurlemann G, Rasic VM, Siskova D, Colomer J, Herczegfalvi A, Fabriciova K, Weschke B, Scola R, Hoellen F, Schara U, Abicht A, Lochmüller H. Mihaylova V, et al. Among authors: salih ma. Brain. 2008 Mar;131(Pt 3):747-59. doi: 10.1093/brain/awm325. Epub 2008 Jan 7. Brain. 2008. PMID: 18180250

6

A novel form of familial congenital muscular dystrophy in two adolescents.

Salih MA, Al Rayess M, Cutshall S, Urtizberea JA, Al-Turaiki MH, Ozo CO, Straub V, Akbar M, Abid M, Andeejani A, Campbell KP. Salih MA, et al. Neuropediatrics. 1998 Dec;29(6):289-93. doi: 10.1055/s-2007-973579. Neuropediatrics. 1998. PMID: 10029346

7

Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entity.

Salih MA, Maisonobe T, Kabiraj M, al Rayess M, al-Turaiki MH, Akbar M, Tahan A, Urtizberea JA, Grid D, Hamadouche T, Guilbot A, Brice A, Leguern E. Salih MA, et al. Neuromuscul Disord. 2000 Jan;10(1):10-5. doi: 10.1016/s0960-8966(99)00057-7. Neuromuscul Disord. 2000. PMID: 10677858

8

Genetic and phenotypic characterization of NKX6-2-related spastic ataxia and hypomyelination.

Chelban V, Alsagob M, Kloth K, Chirita-Emandi A, Vandrovcova J, Maroofian R, Davagnanam I, Bakhtiari S, AlSayed MD, Rahbeeni Z, AlZaidan H, Malintan NT, Johannsen J, Efthymiou S, Ghayoor Karimiani E, Mankad K, Al-Shahrani SA, Beiraghi Toosi M, AlShammari M, Groppa S, Haridy NA, AlQuait L, Qari A, Huma R, Salih MA, Almass R, Almutairi FB, Hamad MH, Alorainy IA, Ramzan K, Imtiaz F, Puiu M, Kruer MC, Bierhals T, Wood NW, Colak D, Houlden H, Kaya N. Chelban V, et al. Among authors: salih ma. Eur J Neurol. 2020 Feb;27(2):334-342. doi: 10.1111/ene.14082. Epub 2019 Oct 17. Eur J Neurol. 2020. PMID: 31509304 Free PMC article.

9

Vaginal ectopic ureter in a duplex system with renal dysplasia. A case report.

Yalçinkaya F, Tümer N, Salih M, Ekim M, Bedük Y, Akyar S, Cakar N, Kansu A. Yalçinkaya F, et al. Among authors: salih m. Int Urol Nephrol. 1994;26(1):7-12. doi: 10.1007/BF02768237. Int Urol Nephrol. 1994. PMID: 8026925

10

Orthostatic proteinuria as a result of venous compression (nutcracker phenomenon)--a hypothesis testable with modern imaging techniques.

Ekim M, Bakkaloglu SA, Tümer N, Sanlidilek U, Salih M. Ekim M, et al. Among authors: salih m. Nephrol Dial Transplant. 1999 Apr;14(4):826-7. doi: 10.1093/ndt/14.4.826. Nephrol Dial Transplant. 1999. PMID: 10328451 No abstract available.

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