Unsuccessful trial of gene replacement in arginase deficiency

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Essential requirement of cytosolic phospholipase A(2) for activation of the H(+) channel in phagocyte-like cells.

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Ferrous and hemoglobin-59Fe absorption from supplemented cow milk in infants with normal and depleted iron stores.

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[The syndrome of inappropriate secretion of antidiuretic hormone and the urinary excretion of aldosterone (author's transl)].

Zeitschrift fur Kinderheilkunde·1975

[Incidence of malignant tumors in childhood (author's transl)].

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Zeitschrift fur Kinderheilkunde·1975

A rare type of low birthweight dwarfism: the Dubowitz syndrome.

Zeitschrift fur Kinderheilkunde·1975

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Unsuccessful trial of gene replacement in arginase deficiency

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Urine analysis performed by flow cytometry: reference range determination and comparison to morphological findings, dipstick chemistry and bacterial culture results--a multicenter study.

Thiopurine methyltransferase activity in the Jewish population of Israel.

Multicenter double-blind, randomized, placebo-controlled trial of levetiracetam as add-on therapy in patients with refractory partial seizures. European Levetiracetam Study Group.

Cytosolic phospholipase A2 is required for the activation of the NADPH oxidase associated H+ channel in phagocyte-like cells.

Antiplatelet treatment does not reduce the severity of subsequent stroke. European Stroke Prevention Study 2 Working Group.

Essential requirement of cytosolic phospholipase A(2) for activation of the H(+) channel in phagocyte-like cells.

Ferrous and hemoglobin-59Fe absorption from supplemented cow milk in infants with normal and depleted iron stores.

[The syndrome of inappropriate secretion of antidiuretic hormone and the urinary excretion of aldosterone (author's transl)].

[Incidence of malignant tumors in childhood (author's transl)].

[Differential diagnosis and follow-up studies in sucklings and infants with continuous cholestasis (author's transl)].

Studies of malformation syndromes in man XXXX: multiple congenital anomalies/mental retardation syndrome or variant familial developmental pattern; differential diagnosis and description of the McDonough syndrome (with XXY son from XY/XXY father).

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Beyond immune rejection: integrative genetic engineering strategies for overcoming coagulopathy in xenotransplantation.

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Unsuccessful trial of gene replacement in arginase deficiency

Abstract:

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