HYPERURICEMIA AND NEUROLOGIC DEFICITS - A FAMILY STUDY

[1] Hereditary familial congenital haemorrhagic nephritis. [J]. BMJ-BRITISH MEDICAL JOURNAL, 1927, 1927 : 504 - 506

[2] MALFORMATION OF THE ERYTHROCYTES IN A CASE OF ATYPICAL RETINITIS PIGMENTOSA [J]. BLOOD, 1950, 5 (04) : 381 - 387

[3] Brown S., 1892, BRAIN, V15, P250

[4] ENGEL WK, 1966, MUSCLE BIOPSY CLINIC, P90

[5] HEREDITARY RENAL DISEASE WITH NEUROSENSORY HEARING LOSS PROLINURIA AND ICHTHYOSIS [J]. AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 1968, 256 (03) : 166 - +

[6] GREENFIELD JG, 1954, SPINO CEREBELLAR DEG, P64

[7] Familial cortical cerebellar atrophy [J]. BRAIN, 1941, 64 : 178 - U24

[8] HEREDITARY PHOTOMYOCLONUS ASSOCIATED WITH DIABETES MELLITUS DEAFNESS NEPHROPATHY + CEREBRAL DYSFUNCTION [J]. NEUROLOGY, 1964, 14 (03) : 212 - +

[9] Holmes G, 1907, BRAIN, V30, P466

[10] HYPOXANTHINE-GUANINE PHOSPHORIBOSYLTRANSFERASE DEFICIENCY IN GOUT [J]. ANNALS OF INTERNAL MEDICINE, 1969, 70 (01) : 155 - +

[1] Hereditary familial congenital haemorrhagic nephritis. [J]. BMJ-BRITISH MEDICAL JOURNAL, 1927, 1927 : 504 - 506

[2] MALFORMATION OF THE ERYTHROCYTES IN A CASE OF ATYPICAL RETINITIS PIGMENTOSA [J]. BLOOD, 1950, 5 (04) : 381 - 387

[3] Brown S., 1892, BRAIN, V15, P250

[4] ENGEL WK, 1966, MUSCLE BIOPSY CLINIC, P90

[5] HEREDITARY RENAL DISEASE WITH NEUROSENSORY HEARING LOSS PROLINURIA AND ICHTHYOSIS [J]. AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 1968, 256 (03) : 166 - +

[6] GREENFIELD JG, 1954, SPINO CEREBELLAR DEG, P64

[7] Familial cortical cerebellar atrophy [J]. BRAIN, 1941, 64 : 178 - U24

[8] HEREDITARY PHOTOMYOCLONUS ASSOCIATED WITH DIABETES MELLITUS DEAFNESS NEPHROPATHY + CEREBRAL DYSFUNCTION [J]. NEUROLOGY, 1964, 14 (03) : 212 - +

[9] Holmes G, 1907, BRAIN, V30, P466

[10] HYPOXANTHINE-GUANINE PHOSPHORIBOSYLTRANSFERASE DEFICIENCY IN GOUT [J]. ANNALS OF INTERNAL MEDICINE, 1969, 70 (01) : 155 - +