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Mutational analysis and genotype/phenotype correlation in Turkish Charcot–Marie–Tooth Type 1 and HNPP patients.
Published in:
Clinical Genetics, 2000, v. 58, n. 5, p. 396, doi. 10.1034/j.1399-0004.2000.580511.x
By:
- Bissar-Tadmouri, N;
- Parman, Y;
- Boutrand, L;
- Deymeer, F;
- Serdaroglu, P;
- Vandenberghe, A;
- Battaloglu, E
Publication type:
Article
Corrigendum: Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.
Published in:
2004
By:
- Züchner, S;
- Mersiyanova, I V;
- Muglia, M;
- Bissar-Tadmouri, N;
- Rochelle, J;
- Dadali, E L;
- Zappia, M;
- Nelis, E;
- Patitucci, A;
- Senderek, J;
- Parman, Y;
- Evgrafov, O;
- Jonghe, P De;
- Takahashi, Y;
- Tsuji, S;
- Pericak-Vance, M A;
- Quattrone, A;
- Battologlu, E;
- Polyakov, A V;
- Timmerman, V
Publication type:
Correction Notice
Reply.
Published in:
Muscle & Nerve, 2012, v. 46, n. 2, p. 296, doi. 10.1002/mus.23328
By:
- Deymeer, F.;
- Matur, Z.;
- Poyraz, M.;
- Battaloglu, E.;
- Oflazer-Serdaroglu, P.;
- Parman, Y.
Publication type:
Article
X-linked Charcot-Marie-Tooth disease and multiple sclerosis.
Published in:
Journal of Neurology, 2007, v. 254, n. 7, p. 953, doi. 10.1007/s00415-006-0324-7
By:
- Parman, Y.;
- Ciftci, F.;
- Poyraz, M.;
- Halefoglu, A.;
- Oge, A.;
- Eraksoy, M.;
- Saruhan-Direskeneli, G.;
- Deymeer, F.;
- Battaloglu, E.
Publication type:
Article
Seventeenth Meeting of the European Neurological Society 16–20 June 2007, Rhodes, Greece.
Published in:
2007
By:
- Argov, Z.;
- Bajenaru, O. A.;
- Baringer, R.;
- Bassetti, C.;
- Cock, H.;
- Comi, G.;
- Dieterich, M.;
- Dietz, V.;
- Eraksoy, M.;
- Fazekas, F.;
- Filippi, M.;
- Hardiman, O.;
- Krarup, C.;
- Lenzi, G. L.;
- Lisak, R.;
- Milonas, I.;
- Moonen, G.;
- Pareyson, D.;
- Parman, Y.;
- Reichmann, H.
Publication type:
Abstract
Charcot-Marie-Tooth disease associated with Type 2 diabetes mellitus.
Published in:
Diabetic Medicine, 2001, v. 18, n. 8, p. 685, doi. 10.1046/j.1464-5491.2001.00530-2.x
By:
- Çelik, M.;
- Forta, H.;
- Parman, Y.;
- Bissar-Tadmouri, N.;
- Demirkirkan, K.;
- Battaloglu, E.
Publication type:
Article
Genetic spectrum of hereditary neuropathies with onset in the first year of life.
Published in:
2011
By:
- Baets J;
- Deconinck T;
- De Vriendt E;
- Zimon M;
- Yperzeele L;
- Van Hoorenbeeck K;
- Peeters K;
- Spiegel R;
- Parman Y;
- Ceulemans B;
- Van Bogaert P;
- Pou-Serradell A;
- Bernert G;
- Dinopoulos A;
- Auer-Grumbach M;
- Sallinen SL;
- Fabrizi GM;
- Pauly F;
- Van den Bergh P;
- Bilir B
Publication type:
journal article
Clinicopathological and genetic study of early-onset demyelinating neuropathy.
Published in:
2004
By:
- Parman Y;
- Battaloglu E;
- Baris I;
- Bilir B;
- Poyraz M;
- Bissar-Tadmouri N;
- Williams A;
- Ammar N;
- Nelis E;
- Timmerman V;
- De Jonghe P;
- Necefov A;
- Deymeer F;
- Serdaroglu P;
- Brophy PJ;
- Said G
Publication type:
Journal Article
Relation of HLA‐DRB1 to IgG4 autoantibody and cytokine production in muscle‐specific tyrosine kinase myasthenia gravis (MuSK‐MG).
Published in:
Clinical & Experimental Immunology, 2019, v. 197, n. 2, p. 214, doi. 10.1111/cei.13302
By:
- Çebi, M.;
- Durmuş, H.;
- Yılmaz, V.;
- Yentür, S.P.;
- Aysal, F.;
- Oflazer, P.;
- Parman, Y.;
- Deymeer, F.;
- Saruhan‐Direskeneli, G.
Publication type:
Article
The effect of interleukin (IL)-21 and CD4+CD25++ T cells on cytokine production of CD4+ responder T cells in patients with myasthenia gravis.
Published in:
Clinical & Experimental Immunology, 2017, v. 190, n. 2, p. 201, doi. 10.1111/cei.13006
By:
- Alahgholi‐Hajibehzad, M.;
- Durmuş, H.;
- Aysal, F.;
- Gülşen‐Parman, Y.;
- Oflazer, P.;
- Deymeer, F.;
- Saruhan‐Direskeneli, G.
Publication type:
Article
Recessive inheritance of a new point mutation of the PMP22 gene in Dejerine-Sottas disease.
Published in:
1999
By:
- Parman, Yesim;
- Planté-Bordeneuve, Violaine;
- Guiochon-Mantel, Anne;
- Eraksoy, Mefkure;
- Said, Gérard;
- Parman, Y;
- Planté-Bordeneuve, V;
- Guiochon-Mantel, A;
- Eraksoy, M;
- Said, G
Publication type:
journal article

Found: 11

Mutational analysis and genotype/phenotype correlation in Turkish Charcot–Marie–Tooth Type 1 and HNPP patients.

Corrigendum: Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.

Reply.

X-linked Charcot-Marie-Tooth disease and multiple sclerosis.

Seventeenth Meeting of the European Neurological Society 16–20 June 2007, Rhodes, Greece.

Charcot-Marie-Tooth disease associated with Type 2 diabetes mellitus.

Genetic spectrum of hereditary neuropathies with onset in the first year of life.

Clinicopathological and genetic study of early-onset demyelinating neuropathy.

Relation of HLA‐DRB1 to IgG4 autoantibody and cytokine production in muscle‐specific tyrosine kinase myasthenia gravis (MuSK‐MG).

The effect of interleukin (IL)-21 and CD4<sup>+</sup>CD25<sup>++</sup> T cells on cytokine production of CD4<sup>+</sup> responder T cells in patients with myasthenia gravis.

Recessive inheritance of a new point mutation of the PMP22 gene in Dejerine-Sottas disease.