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Lesch-Nyhan syndrome: a novel complex mutation with severe phenotype.
Published in:
Clinical Genetics, 2010, v. 78, n. 3, p. 296, doi. 10.1111/j.1399-0004.2010.01428.x
By:
- Gucev, Z.;
- Koceva, S.;
- Marinaki, A.;
- Fairbanks, L.;
- Kirovski, I.;
- Tasic, V.
Publication type:
Article
Ceftriaxone associated urolithiasis in a child with hypercalciuria.
Published in:
2011
By:
- Lozanovski, V. J.;
- Gucev, Z.;
- Avramoski, V. J.;
- Kirovski, I.;
- Makreski, P.;
- Tasic, V.
Publication type:
Case Study
A GIANT OSTEOCHONDROMA IN A BOY WITH MULTIPLE EXOSTOSES.
Published in:
Contributions of Macedonian Academy of Sciences & Arts, 2011, v. 32, n. 2, p. 317
By:
- I., Kirovski;
- Z. S., Gucev;
- V., Tasic;
- N., Pop-Jordanova
Publication type:
Article
FOUR GENERATIONS IN A FAMILY WITH NEUROFIBROMATOSIS 1: PRECOCIOUS PUBERTY AND OPTIC NERVE TUMOR (OPT).
Published in:
2010
By:
- Z., Gucev;
- M., Krstevska-Konstantinova;
- V., Tasic;
- A., Jancevska;
- I., Kirovski;
- N., Pop-Jordanova
Publication type:
Case Study
TYPE I GAUCHER DISEASE (GDI) IN THREE SIBLINGS: ENZYME REPLACEMENT TREATMENT (ERT) REQUIRED.
Published in:
Contributions of Macedonian Academy of Sciences & Arts, 2009, v. 30, n. 1, p. 233
By:
- Gucev, Z. S.;
- Tasic, V.;
- Pop-Jordanova, N.;
- Kirovski, I.;
- Stomnaroska, O.;
- Martinova, M.;
- Jancevska, A.;
- Kremensky, I.;
- Sinigerska, I.
Publication type:
Article