Treatment of homozygous protein C deficiency and neonatal purpura fulminans with a purified protein C concentrate.

Neonatal purpura fulminans associated with homozygous protein S deficiency.

Neonatal purpura fulminans and transient protein C deficiency.

Neonatal purpura fulminans due to protein C deficiency.

Neonatal purpura fulminans due to homozygous protein C or protein S deficiencies.

Homozygous protein S deficiency in an infant with purpura fulminans.

Asymptomatic homozygous protein C deficiency.

Late-onset homozygous protein C deficiency.

Subcutaneous protein C concentrate in the management of severe protein C deficiency--experience from 12 centres.

Successful treatment of neonatal purpura fulminans with epoprostenol.

Continuous subcutaneous infusion of protein C concentrate using an insulin pump in a newborn with congenital protein C deficiency.

Protein C survival during replacement therapy in homozygous protein C deficiency.

Successful treatment of neonatal purpura fulminans with epoprostenol.

Acquired transient protein C deficiency in neonatal cardiac failure.

Protein C deficiency.

Pregnancy and protein C deficiency.

Homozygous protein C deficiency with late onset and recurrent coumarin-induced skin necrosis.

Cerebral infarction associated with protein C deficiency.

Stroke in protein C deficiency.

Surgical treatment of pulmonary hypertension in protein C deficiency.

Molecular basis of hereditary protein C and protein S deficiency.

A novel mutation c.1048A>T at codon 350(Lys>Stop) in PROC gene causing neonatal purpura fulminans.

Concurrent protein C deficiency and lupus anticoagulants.

Late-onset homozygous protein C deficiency manifesting cerebral infarction as the first symptom at age 27.

Purpura fulminans.

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Neonatal purpura fulminans associated with homozygous protein S deficiency.

Neonatal purpura fulminans and transient protein C deficiency.

Neonatal purpura fulminans due to protein C deficiency.

Neonatal purpura fulminans due to homozygous protein C or protein S deficiencies.

Homozygous protein S deficiency in an infant with purpura fulminans.

Asymptomatic homozygous protein C deficiency.

Late-onset homozygous protein C deficiency.

Subcutaneous protein C concentrate in the management of severe protein C deficiency--experience from 12 centres.

Successful treatment of neonatal purpura fulminans with epoprostenol.

Continuous subcutaneous infusion of protein C concentrate using an insulin pump in a newborn with congenital protein C deficiency.

Protein C survival during replacement therapy in homozygous protein C deficiency.

Successful treatment of neonatal purpura fulminans with epoprostenol.

Acquired transient protein C deficiency in neonatal cardiac failure.

Protein C deficiency.

Pregnancy and protein C deficiency.

Homozygous protein C deficiency with late onset and recurrent coumarin-induced skin necrosis.

Cerebral infarction associated with protein C deficiency.

Stroke in protein C deficiency.

Surgical treatment of pulmonary hypertension in protein C deficiency.

Molecular basis of hereditary protein C and protein S deficiency.

A novel mutation c.1048A>T at codon 350(Lys>Stop) in PROC gene causing neonatal purpura fulminans.

Concurrent protein C deficiency and lupus anticoagulants.

Late-onset homozygous protein C deficiency manifesting cerebral infarction as the first symptom at age 27.

Purpura fulminans.

Treatment of homozygous protein C deficiency and neonatal purpura fulminans with a purified protein C concentrate.

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