Volume 8; Issue 3

Molecular Diagnosis & Therapy

Volume 8; Issue 3

1

Catalase enzyme mutations and their association with diseases

Góth, László, Rass, Péter, Páy, Anikó

Journal:

Molecular Diagnosis & Therapy

Year:

2004

Language:

english

File:

PDF, 126 KB

english, 2004

2

Hereditary hyperekplexia caused by novel mutations ofGLRA1in Turkish families

Gilbert, Sandra L., Ozdag, Fatih, Ulas, Umit H., Dobyns, William B., Lahn, Bruce T.

Journal:

Molecular Diagnosis & Therapy

Year:

2004

Language:

english

File:

PDF, 149 KB

english, 2004

3

Association of the human bradykinin B2receptor gene with chronic renal failure

Lucyna Jozwiak,Andrzej Drop,Kinga Buraczynska,Piotr Ksiazek…

Journal:

Molecular Diagnosis & Therapy

Year:

2004

Language:

english

File:

PDF, 97 KB

english, 2004

4

A novel 1297–1304delGCCTGCCA mutation in the exon 10 of the thyroid hormone receptor β gene causes resistance to thyroid hormone

Carina M. Rivolta,M. Susana Mallea Gil,Carolina Ballarino…

Journal:

Molecular Diagnosis & Therapy

Year:

2004

Language:

english

File:

PDF, 177 KB

english, 2004

5

17α-hydroxylase deficiency

Maria S. Perez,Haydee Benencia,Dr Gustavo D. Frechtel…

Journal:

Molecular Diagnosis & Therapy

Year:

2004

Language:

english

File:

PDF, 181 KB

english, 2004

6

Quantitative detection ofEscherichia colifrom urine of patients with bacteriuria by real-time PCR

Nobuyuki Hinata,Dr Toshiro Shirakawa,Hiroshi Okada…

Journal:

Molecular Diagnosis & Therapy

Year:

2004

Language:

english

File:

PDF, 117 KB

english, 2004

7

Comparison of three PCR assays for the evaluation of interferon-β biological activity in patients with multiple sclerosis

Dr Francesca Gilli,Fabiana Marnetto,Guglielmo Stefanuto…

Journal:

Molecular Diagnosis & Therapy

Year:

2004

Language:

english

File:

PDF, 189 KB

english, 2004