Kozich V - Search Results

1

Unusual clinical presentation in two boys with cytochrome c oxidase deficiency.

Hrebícek M, Zeman J, Petrák B, Kozich V, Hyánek J, Ruiter JP, Wanders RJ, Wijburg FA. Hrebícek M, et al. Among authors: kozich v. J Inherit Metab Dis. 1992;15(3):320-2. doi: 10.1007/BF02435966. J Inherit Metab Dis. 1992. PMID: 1357227 No abstract available.

2

Mevalonic aciduria.

Kozich V, Gibson KM, Zeman J, Nĕmecek J, Hoffman GF, Pehal F, Hyánek J, Grosmanová A, Verner P. Kozich V, et al. J Inherit Metab Dis. 1991;14(2):265-6. doi: 10.1007/BF01800602. J Inherit Metab Dis. 1991. PMID: 1653382 No abstract available.

3

[Non-ketotic hyperglycinemia].

Zeman J, Kozich V, Stastná S, Hyánek J, Hoza J, Rajecký J, Verner P, Pehal F. Zeman J, et al. Among authors: kozich v. Cesk Pediatr. 1990 Nov;45(11):671-2. Cesk Pediatr. 1990. PMID: 1709392 Czech. No abstract available.

4

Di- and trihydroxycholestanaemia in twin sisters.

Wanders RJ, van Roermund CW, Schelen A, Schutgens RB, Zeman J, Kozich V, Hyanek J, Casteels M, Mannaerts GP. Wanders RJ, et al. Among authors: kozich v. J Inherit Metab Dis. 1991;14(3):357-60. doi: 10.1007/BF01811702. J Inherit Metab Dis. 1991. PMID: 1770791 No abstract available.

5

Accumulation and impaired in vivo metabolism of di- and trihydroxycholestanoic acid in two patients.

Wanders RJ, Casteels M, Mannaerts GP, van Roermund CW, Schutgens RB, Kozich V, Zeman J, Hyanek J. Wanders RJ, et al. Among authors: kozich v. Clin Chim Acta. 1991 Oct 31;202(3):123-32. doi: 10.1016/0009-8981(91)90043-c. Clin Chim Acta. 1991. PMID: 1839974

6

[Phosphoethanolamine in the blood and urine in sick children].

Zeman L, Zeman J, Kozich V, Matousová M, Velísková J. Zeman L, et al. Among authors: kozich v. Cesk Pediatr. 1991 Jan;46(1):19-22. Cesk Pediatr. 1991. PMID: 1884405 Czech.

7

[Peroxisomal disorders--is diagnosis possible in Czechoslovakia?].

Hyánek J, Kozich V, Pehal F. Hyánek J, et al. Among authors: kozich v. Cesk Pediatr. 1990 Jan;45(1):51-2. Cesk Pediatr. 1990. PMID: 2393931 Czech. No abstract available.

8

[Maternal hyperphenylalaninemia in a population of healty Czech women. 18 years' experience with mass screening, diet therapy and metabolic monitoring].

Hyánek J, Bendl J, Zeman J, Soukup K, Dolezal A, Kozich V, St'astná S, Kubík M, Viletová H. Hyánek J, et al. Among authors: kozich v. Cas Lek Cesk. 1996 Jan 17;135(2):50-3. Cas Lek Cesk. 1996. PMID: 8616880 Czech.

9

Analysis of CBS alleles in Czech and Slovak patients with homocystinuria: report on three novel mutations E176K, W409X and 1223 + 37 del99.

Kozich V, Janosík M, Sokolová J, Oliveriusová J, Orendác M, Kraus JP, Elleder D. Kozich V, et al. J Inherit Metab Dis. 1997 Jul;20(3):363-6. doi: 10.1023/a:1005325911665. J Inherit Metab Dis. 1997. PMID: 9266356 Clinical Trial. No abstract available.

10

Unusual enzyme findings in five patients with metabolic profiles suggestive of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria).

Gibson KM, Sweetman L, Kozich V, Pijackova A, Tscharre A, Cortez A, Eyskens F, Jakobs C, Duran M, Poll-The BT. Gibson KM, et al. Among authors: kozich v. J Inherit Metab Dis. 1998 Jun;21(3):255-61. doi: 10.1023/a:1005368106563. J Inherit Metab Dis. 1998. PMID: 9686370 No abstract available.

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