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Haemostatic studies in carbohydrate-deficient glycoprotein syndrome type I

Thrombosis and haemostasis, 1996-10, Vol.76 (4), p.502-504

1996

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Carbohydrate deficient glycoprotein syndrome type I: ophthalmic aspects in four Sicilian patients

British journal of ophthalmology, 1994-11, Vol.78 (11), p.845-846

1994

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Phenotypic variability and abnormal type I collagen unstable at body temperature in a family with mild dominant osteogenesis imperfecta

Journal of inherited metabolic disease, 1991-03, Vol.14 (2), p.189-201

1991

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Contribution to the pyretotherapy of chorea minor

La Clinica pediatrica, 1962-10, Vol.44, p.721

BUTTITTA, P

1962

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On neuro-psychic sequelae in children born by difficult delivery

Minerva nipiologica, 1962-11, Vol.12, p.412

BUTTITTA, P

1962

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Olivopontocerebellar atrophy leading to recognition of carbohydrate-deficient glycoprotein syndrome type I

Journal of neurology, 1996-10, Vol.243 (10), p.700-705

1996

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Biology of Toxoplasma hominis in the guinea pig, mouse and embryonated egg

Bollettino della Societa italiana di biologia sperimentale, 1951-01, Vol.27 (1-2), p.83

BUTTITTA, P L

1951

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Complement fixing antigens in toxoplasmosis

Bollettino della Societa italiana di biologia sperimentale, 1952-03, Vol.28 (3), p.332

BUTTITTA, P L

1952

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Diagnostic value of agglutination test in rickettsiosis

Bollettino della Societa italiana di biologia sperimentale, 1951-01, Vol.27 (1-2), p.86

BUTTITTA, P L

1951

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Isolation in the mouse and in embryonated egg of a strain of Toxoplasma hominis from the cerebrospinal fluid of a patient with positive cutaneous & stain reactions

Bollettino della Societa italiana di biologia sperimentale, 1951-01, Vol.27 (1-2), p.83

BUTTITTA, P L

1951

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Characteristics of a focus of endemic exanthematous typhus in the province of Palermo

Bollettino della Societa italiana di biologia sperimentale, 1951-01, Vol.27 (1-2), p.85

BUTTITTA, P L

1951

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New technic for agglutination with Rickettsia burneti

Bollettino della Societa italiana di biologia sperimentale, 1950-07, Vol.26 (8), p.1353

BUTTITTA, P L

1950

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Adaptability to culture in embryonated egg of strains of Rickettsia burneti isolated in western Sicily

Bollettino della Societa italiana di biologia sperimentale, 1950-07, Vol.26 (8), p.1349

BUTTITTA, P L

1950

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Epidemiological research on boutonneuse fever in Palermo

Bollettino della Societa italiana di biologia sperimentale, 1950-07, Vol.26 (8), p.1350

BUTTITTA, P L

1950

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Acute experimental peritonitis in the guinea pig from Rickettsia burneti

Bollettino della Societa italiana di biologia sperimentale, 1950-07, Vol.26 (8), p.1352

BUTTITTA, P L

1950

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MLO's national CLIA '88 survey, Part I: The self-assessment survey

MLO. Medical laboratory observer, 1998-01, Vol.30 (1), p.36

1998

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Mild dominant osteogenesis imperfecta with intrafamilial variability : the cause is a serine for glycine α1(I) 901 substitution in a type-I collagen gene

Human genetics, 1992-07, Vol.89 (5), p.480-484

1992

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Further epidemiological and serological research on western equine encephalitis

Bollettino della Societa italiana di biologia sperimentale, 1952-07, Vol.28 (7), p.1534

1952

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Observations of complement deviation according to Kolmer

Bollettino della Societa italiana di biologia sperimentale, 1952-07, Vol.28 (7), p.1552

1952

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Further epidemiological and serological research on Q fever

Bollettino della Societa italiana di biologia sperimentale, 1952-07, Vol.28 (7), p.1533

1952

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Sulfamide resistance of Flexner bacillus

Bollettino della Societa italiana di biologia sperimentale, 1952-06, Vol.28 (6), p.1210

1952

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Focus of rickettsiosis burneti of exclusively febrile form and without trace of pulmonary infiltration

Bollettino della Societa italiana di biologia sperimentale, 1951-01, Vol.27 (1-2), p.87

1951

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MLO's survey of computer use in the laboratory

MLO. Medical laboratory observer, 1998-08, Vol.30 (8), p.56

1998

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Holoprosencephaly: Examples of clinical variability and etiologic heterogeneity

American journal of medical genetics, 1990-10, Vol.37 (2), p.244-249

1990

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Roberts syndrome: phenotypic variation, cytogenetic definition and heterozygote detection

Annales de génétique, 1991, Vol.34 (3-4), p.239

1991

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Haemostatic studies in carbohydrate-deficient glycoprotein syndrome type I

Carbohydrate deficient glycoprotein syndrome type I: ophthalmic aspects in four Sicilian patients

Phenotypic variability and abnormal type I collagen unstable at body temperature in a family with mild dominant osteogenesis imperfecta

Contribution to the pyretotherapy of chorea minor

On neuro-psychic sequelae in children born by difficult delivery

Olivopontocerebellar atrophy leading to recognition of carbohydrate-deficient glycoprotein syndrome type I

Biology of Toxoplasma hominis in the guinea pig, mouse and embryonated egg

Complement fixing antigens in toxoplasmosis

Diagnostic value of agglutination test in rickettsiosis

Isolation in the mouse and in embryonated egg of a strain of Toxoplasma hominis from the cerebrospinal fluid of a patient with positive cutaneous & stain reactions

Characteristics of a focus of endemic exanthematous typhus in the province of Palermo

New technic for agglutination with Rickettsia burneti

Adaptability to culture in embryonated egg of strains of Rickettsia burneti isolated in western Sicily

Epidemiological research on boutonneuse fever in Palermo

Acute experimental peritonitis in the guinea pig from Rickettsia burneti

MLO's national CLIA '88 survey, Part I: The self-assessment survey

Mild dominant osteogenesis imperfecta with intrafamilial variability : the cause is a serine for glycine α1(I) 901 substitution in a type-I collagen gene

Further epidemiological and serological research on western equine encephalitis

Observations of complement deviation according to Kolmer

Further epidemiological and serological research on Q fever

Sulfamide resistance of Flexner bacillus

Focus of rickettsiosis burneti of exclusively febrile form and without trace of pulmonary infiltration

MLO's survey of computer use in the laboratory

Holoprosencephaly: Examples of clinical variability and etiologic heterogeneity

Roberts syndrome: phenotypic variation, cytogenetic definition and heterozygote detection

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