BIOCHEMICAL OBSERVATIONS ON SO-CALLED HEREDITARY TYROSINEMIA

[1] HEREDITARY TYROSINEMIA .3. ON DIFFERENTIAL DIAGNOSIS AND LACK OF EFFECT OF EARLY DIETARY TREATMENT [J]. ACTA PAEDIATRICA SCANDINAVICA, 1969, 58 (01): : 37 - +

[2] HOMOCYSTINURIA - METABOLIC STUDIES ON 3 PATIENTS [J]. JOURNAL OF PEDIATRICS, 1965, 67 (01) : 58 - +

[3] CUSWORTH DC, 1966, LANCET, V1, P598

[4] GAULL G E, 1969, Neuropaediatrie, V1, P199, DOI 10.1055/s-0028-1091874

[5] GAULL GE, 1968, PEDIATR RES, V2, P403

[6] GAULL GE, 1968, LANCET, V1, P1317

[7] EXCRETION OF DELTA-AMINOLEVULINIC ACID IN HEREDITARY TYROSINEMIA [J]. CLINICA CHIMICA ACTA, 1969, 23 (02) : 257 - +

[8] TYROSINEMIA - AN INBORN ERROR OF TYROSINE METABOLISM WITH CIRRHOSIS OF LIVER AND MULTIPLE RENAL TUBULAR DEFECTS ( DE TONI-DEBRE-FANCONI SYNDROME ) [J]. JOURNAL OF PEDIATRICS, 1965, 66 (04) : 670 - +

[9] ENZYMATIC STUDIES IN A CASE OF HEREDITARY TYROSINEMIA WITH HEPATOMA [J]. ACTA PAEDIATRICA SCANDINAVICA, 1969, 58 (04): : 393 - +

[10] GJESSING LR, 1965, LANCET, V2, P1132

[1] HEREDITARY TYROSINEMIA .3. ON DIFFERENTIAL DIAGNOSIS AND LACK OF EFFECT OF EARLY DIETARY TREATMENT [J]. ACTA PAEDIATRICA SCANDINAVICA, 1969, 58 (01): : 37 - +

[2] HOMOCYSTINURIA - METABOLIC STUDIES ON 3 PATIENTS [J]. JOURNAL OF PEDIATRICS, 1965, 67 (01) : 58 - +

[3] CUSWORTH DC, 1966, LANCET, V1, P598

[4] GAULL G E, 1969, Neuropaediatrie, V1, P199, DOI 10.1055/s-0028-1091874

[5] GAULL GE, 1968, PEDIATR RES, V2, P403

[6] GAULL GE, 1968, LANCET, V1, P1317

[7] EXCRETION OF DELTA-AMINOLEVULINIC ACID IN HEREDITARY TYROSINEMIA [J]. CLINICA CHIMICA ACTA, 1969, 23 (02) : 257 - +

[8] TYROSINEMIA - AN INBORN ERROR OF TYROSINE METABOLISM WITH CIRRHOSIS OF LIVER AND MULTIPLE RENAL TUBULAR DEFECTS ( DE TONI-DEBRE-FANCONI SYNDROME ) [J]. JOURNAL OF PEDIATRICS, 1965, 66 (04) : 670 - +

[9] ENZYMATIC STUDIES IN A CASE OF HEREDITARY TYROSINEMIA WITH HEPATOMA [J]. ACTA PAEDIATRICA SCANDINAVICA, 1969, 58 (04): : 393 - +

[10] GJESSING LR, 1965, LANCET, V2, P1132