The occurrence of hepatoma in the chronic form of hereditary tyrosinemia
AG Weinberg, CE Mize, HG Worthen - The Journal of pediatrics, 1976 - Elsevier
A 5 1/2-year-old child with hepatocarcinoma complicating hereditary tyrosinemia is
presented. A review of the literature and an attempted follow-up of previously reported …
presented. A review of the literature and an attempted follow-up of previously reported …
Hepatorenal tyrosinemia
T Kitagawa - Proceedings of the Japan Academy, Series B, 2012 - jstage.jst.go.jp
In 1957 Sakai and Kitagawa in Japan reported the clinical and biochemical findings in a
patient with tyrosinemia, tyrosyluria, liver cirrhosis, and renal rickets. Subsequently, reports …
patient with tyrosinemia, tyrosyluria, liver cirrhosis, and renal rickets. Subsequently, reports …
Hereditary tyrosinemia in a French Canadian isolate.
C Laberge - American Journal of Human Genetics, 1969 - ncbi.nlm.nih.gov
RESULTS The Genetics All sibships of hereditary tyrosinemia ascertained in the isolate are
shownin Figure 2 according to time of first appearance and decreasing family size. Sibships …
shownin Figure 2 according to time of first appearance and decreasing family size. Sibships …
Urinary phenolic acids in tyrosinemia. identification and quantitation by gas chromatographymass spectrometry
JC Crawhall, O Mamer, S Tjoa, JC Claveau - Clinica Chimica Acta, 1971 - Elsevier
The urinary phenolic acids from two patients with tyrosinemia being treated with low tyrosine-
phenylalanine diets and from four normal controls were analysed by paper chromatography …
phenylalanine diets and from four normal controls were analysed by paper chromatography …
Hereditary tyrosinemia with hyperplasia and hypertrophy of juxtaglomerular apparatus
MM Jevtic, FK Thorp, Z Hruban - American Journal of Clinical …, 1974 - academic.oup.com
Histopathologic and clinical studies of a child with the acute form of hereditary tyrosinemia
indicate the difficulty in distinguishing certain features of this disorder from those of …
indicate the difficulty in distinguishing certain features of this disorder from those of …
[BOOK][B] Advances in human genetics
H Harris, K Hirschhorn - 1970 - Springer
1 2 2 4 7 7 8 9 9 Qualitative Genetic Variation 12 Variants of Human Carbonic Anhydrase I
12 Variants of Human Carbonic Anhydrase II 21 Carbonic Anhydrase Variants in Nonhuman …
12 Variants of Human Carbonic Anhydrase II 21 Carbonic Anhydrase Variants in Nonhuman …
Population genetics and health care delivery: the Quebec experience
C Laberge - Advances in Human Genetics 6, 1976 - Springer
The main objective of this chapter is to define the potentialities for genetic studies in the
French Canadians. Different levels of approach to the problem have been tried in the last 6 …
French Canadians. Different levels of approach to the problem have been tried in the last 6 …
Recovery after dietary treatment of an infant with features of tyrosinosis.
JT Harries, JW Seakins, RS Ersser… - Archives of Disease in …, 1969 - ncbi.nlm.nih.gov
Tyrosinosis has been recognized with increasing frequency in recent years, and the disease
is characterized by cirrhosis of the liver, renal tubular dysfunction, and hypophosphataemic …
is characterized by cirrhosis of the liver, renal tubular dysfunction, and hypophosphataemic …
[BOOK][B] Genetic studies in French Canadians
CMJ Laberge - 1968 - search.proquest.com
University Microfilms, Inc., Ann Arbor, Michigan Page 1 This dissertation has been microfilmed
exactly as received 6 8 -1 6 ,4 4 0 LABERGE, Claude Marie Joseph, 1938GENETIC STUDIES IN …
exactly as received 6 8 -1 6 ,4 4 0 LABERGE, Claude Marie Joseph, 1938GENETIC STUDIES IN …
Tyrosinosis: Primary and secondary metabolic disturbances
W Nützenadel, P Lutz, H Bickel - Zeitschrift für Kinderheilkunde, 1972 - Springer
A child with so-called “tyrosinosis” was treated with a reduced phenylalanine and tyrosine
intake (100 mg/kg/day) for two periods of 2 and 9 months each. Healing of rickets …
intake (100 mg/kg/day) for two periods of 2 and 9 months each. Healing of rickets …
