STUDIES ON ALCAPTONURIA .2. INVESTIGATIONS ON A CASE OF HUMAN ALCAPTONURIA

[21] KATSCH G, 1918, DEUT ARCH KLIN MED, V127, P210

[22] LANGSTEIN L, 1903, DTSCH ARCH KLIN MED, V78, P161

[23] Decomposition of d- and l-form of phenylalanine and the d,l- and l-form of tyrosin through the alcapton uriker [J]. HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1942, 275 : 217 - 224

[24] The quantitative determination of the homogentisine acidsin blood serum and in the milk of alkaptonurics. [J]. HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1931, 203 : 135 - 141

[25] Alkaptonuria with hyperuricemia [J]. ARCHIVES OF INTERNAL MEDICINE, 1943, 71 (01) : 68 - 77

[26] A defect in the metabolism of tyrosine and phenylalanine in premature infants. I. Identification and assay of intermediary products [J]. JOURNAL OF CLINICAL INVESTIGATION, 1941, 20 (02) : 199 - 207

[27] A defect in the metabolism of tyrosine and phenylalanine in premature infants. II. Spontaneous occurrence and eradication by vitamin C [J]. JOURNAL OF CLINICAL INVESTIGATION, 1941, 20 (02) : 209 - 219

[28] Alcaptonuria during minimal protein supply. [J]. HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1930, 186 : 111 - 118

[29] LORENZ E, 1937, KLIN WOCHENSCHR, V16, P1463

[30] MCCANCE RA, 1940, SPEC REP SER MED RES, V235

[21] KATSCH G, 1918, DEUT ARCH KLIN MED, V127, P210

[22] LANGSTEIN L, 1903, DTSCH ARCH KLIN MED, V78, P161

[23] Decomposition of d- and l-form of phenylalanine and the d,l- and l-form of tyrosin through the alcapton uriker [J]. HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1942, 275 : 217 - 224

[24] The quantitative determination of the homogentisine acidsin blood serum and in the milk of alkaptonurics. [J]. HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1931, 203 : 135 - 141

[25] Alkaptonuria with hyperuricemia [J]. ARCHIVES OF INTERNAL MEDICINE, 1943, 71 (01) : 68 - 77

[26] A defect in the metabolism of tyrosine and phenylalanine in premature infants. I. Identification and assay of intermediary products [J]. JOURNAL OF CLINICAL INVESTIGATION, 1941, 20 (02) : 199 - 207

[27] A defect in the metabolism of tyrosine and phenylalanine in premature infants. II. Spontaneous occurrence and eradication by vitamin C [J]. JOURNAL OF CLINICAL INVESTIGATION, 1941, 20 (02) : 209 - 219

[28] Alcaptonuria during minimal protein supply. [J]. HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1930, 186 : 111 - 118

[29] LORENZ E, 1937, KLIN WOCHENSCHR, V16, P1463

[30] MCCANCE RA, 1940, SPEC REP SER MED RES, V235