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Decreasing choline signal--a marker of phenylketonuria?
Dezortová M, Hejcmanová L, Hájek M. Dezortová M, et al. Among authors: hejcmanova l. MAGMA. 1996 Sep-Dec;4(3-4):181-6. doi: 10.1007/BF01772005. MAGMA. 1996. PMID: 9220406
MR in phenylketonuria-related brain lesions.
Dezortová M, Hájek M, Tintera J, Hejcmanová L, Syková E. Dezortová M, et al. Among authors: hejcmanova l. Acta Radiol. 2001 Sep;42(5):459-66. Acta Radiol. 2001. PMID: 11552882
Proton in vivo spectroscopy of patients with hyperphenylalaninaemia.
Hájek M, Hejcmanová L, Prádný J. Hájek M, et al. Among authors: hejcmanova l. Neuropediatrics. 1993 Apr;24(2):111-2. doi: 10.1055/s-2008-1071525. Neuropediatrics. 1993. PMID: 8327063
[Triplets, 2 of which are twins with phenylketonuria].
Blehová B, Pazoutová N, Hejcmanová L, Milunicová A, Jirásek J. Blehová B, et al. Among authors: hejcmanova l. Cesk Pediatr. 1975 Dec;30(12):587-8. Cesk Pediatr. 1975. PMID: 1240020 Czech. No abstract available.
[Characteristics of hemodynamics in juvenile hypertension].
Ringel J, Palyzová D, Hejcmanová L. Ringel J, et al. Among authors: hejcmanova l. Cesk Pediatr. 1978 Nov;33(11):672-7. Cesk Pediatr. 1978. PMID: 737817 Czech. No abstract available.
A unique RFLP haplotype at the phenylalanine hydroxylase locus in Czechoslovak Gypsies with phenylketonuria.
Feráková E, Ferák V, Kádasi L, Poláková H, Hejcmanová L, Pijacková A. Feráková E, et al. Among authors: hejcmanova l. Funct Dev Morphol. 1992;2(2):139-40. Funct Dev Morphol. 1992. PMID: 1360274 No abstract available.
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