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Value of histochemical stains for copper in the diagnosis of Wilson's disease

Histopathology, 1998-07, Vol.33 (1), p.28-33

1998

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A distal renal tubular acidosis showing hyperammonemia and hyperlactacidemia

La Pediatria medica e chirurgica, 2012-07, Vol.34 (4), p.198-201

2012

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Molecular characterization of Wilson disease in the Sardinian population-Evidence of a founder effect

Human mutation, 1999-01, Vol.14 (4), p.294-303

1999

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Epidemiologic study of hepatolenticular degeneration (Wilson's disease) in Sardinia (1902-1983)

Acta neurologica Scandinavica, 1985-07, Vol.72 (1), p.43-55

1985

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Carrier detection and early diagnosis of Wilson's disease by restriction fragment length polymorphism analysis

Journal of medical genetics, 1989-02, Vol.26 (2), p.78-82

1989

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Adrenal androgens in obese boys before and after weight loss

Hormone and metabolic research, 1984-10, Vol.16 (10), p.544-548

1984

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Sexual maturation and adrenal function in girls with thalassemia

Journal of endocrinological investigation, 1984-06, Vol.7 (3), p.181-184

1984

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Adrenal and testicular function in boys affected by thalassemia

Journal of endocrinological investigation, 1984-04, Vol.7 (2), p.147-149

1984

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Computerized cranial tomography in presymptomatic and hepatic form of Wilson's disease

European neurology, 1984, Vol.23 (1), p.56-63

1984

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Congenital hepatic dysplasia from cytomegalovirus

Pathologica, 1993-01, Vol.85 (1095), p.91

1993

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Rapid Identification of Wilson's Disease Carriers by Denaturing High-Performance Liquid Chromatography

Preventive medicine, 2002-09, Vol.35 (3), p.278-284

2002

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A genetic combination of silent beta-thalassaemia, high Hb A2 beta-thalassaemia, and single alpha globin gene deletion causing mild thalassaemia intermedia

Journal of medical genetics, 1984-04, Vol.21 (2), p.153-156

1984

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Simple or benign febrile convulsions. Clinical and statistical evaluation

Minerva pediatrica, 1982-02, Vol.34 (4), p.179

1982

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Importance and significance of liver echotomography in Wilson's disease during childhood

The Journal of nuclear medicine and allied sciences, 1987-07, Vol.31 (3), p.231

1987

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Hepatic echographic scanning in thalassemia major

The Journal of nuclear medicine and allied sciences, 1984-07, Vol.28 (3), p.143

1984

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Diagnostic value of histochemical stains for copper in Wilson's disease

Journal of hepatology, 1998, Vol.28, p.134-134

1998

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Osteomatosis of the skin. Presentation of 2 cases

Pathologica, 1989-01, Vol.81 (1071), p.103

1989

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Behavior of the electroencephalographic examination in the acute period and in the follow-up of purulent meningitis in children

Minerva pediatrica, 1981-09, Vol.33 (18), p.891

1981

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A genetic combination of silent beta -thalassaemia, high Hb A sub(2) beta -thalassaemia, and single alpha globin gene deletion causing mild thalassaemia intermedia

Journal of medical genetics, 1984-01, Vol.21 (2), p.153-156

1984

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A genetic combination of silent β-thalassaemia, high Hb A2 β-thalassaemia, and single α globin gene deletion causing mild thalassaemia intermadia

Journal of medical genetics, 1984, Vol.21 (2), p.153-156

1984

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Acute disseminated histiocytosis X. Presentation of a case

Pathologica, 1989-05, Vol.81 (1073), p.325

1989

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Psychological aspects of the epileptic child and his relationship to his family environment

La Pediatria medica e chirurgica, 1984-01, Vol.6 (1), p.109

1984

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Syndactylia associated with multiple malformation syndromes. Observation of a new symptomatologic complex in 3 brothers

La Pediatria medica e chirurgica, 1988-03, Vol.10 (2), p.227

1988

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Adrenal androgens in obese boys before and after weight loss

Hormone and metabolic research, 1984, Vol.10 (16), p.544-548

1984

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Children and illness

La Pediatria medica e chirurgica, 1982-05, Vol.4 (3), p.303

1982

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Value of histochemical stains for copper in the diagnosis of Wilson's disease

A distal renal tubular acidosis showing hyperammonemia and hyperlactacidemia

Molecular characterization of Wilson disease in the Sardinian population-Evidence of a founder effect

Epidemiologic study of hepatolenticular degeneration (Wilson's disease) in Sardinia (1902-1983)

Carrier detection and early diagnosis of Wilson's disease by restriction fragment length polymorphism analysis

Adrenal androgens in obese boys before and after weight loss

Sexual maturation and adrenal function in girls with thalassemia

Adrenal and testicular function in boys affected by thalassemia

Computerized cranial tomography in presymptomatic and hepatic form of Wilson's disease

Congenital hepatic dysplasia from cytomegalovirus

Rapid Identification of Wilson's Disease Carriers by Denaturing High-Performance Liquid Chromatography

A genetic combination of silent beta-thalassaemia, high Hb A2 beta-thalassaemia, and single alpha globin gene deletion causing mild thalassaemia intermedia

Simple or benign febrile convulsions. Clinical and statistical evaluation

Importance and significance of liver echotomography in Wilson's disease during childhood

Hepatic echographic scanning in thalassemia major

Diagnostic value of histochemical stains for copper in Wilson's disease

Osteomatosis of the skin. Presentation of 2 cases

Behavior of the electroencephalographic examination in the acute period and in the follow-up of purulent meningitis in children

A genetic combination of silent beta -thalassaemia, high Hb A sub(2) beta -thalassaemia, and single alpha globin gene deletion causing mild thalassaemia intermedia

A genetic combination of silent β-thalassaemia, high Hb A2 β-thalassaemia, and single α globin gene deletion causing mild thalassaemia intermadia

Acute disseminated histiocytosis X. Presentation of a case

Psychological aspects of the epileptic child and his relationship to his family environment

Syndactylia associated with multiple malformation syndromes. Observation of a new symptomatologic complex in 3 brothers

Adrenal androgens in obese boys before and after weight loss

Children and illness

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