Search Results - "Havass, Z"

Neonatal screening for biotinidase deficiency in Hungary: Clinical, biochemical and molecular studies by László, Á., Schuler, É. Á., Sallay, É., Endreffy, E., Somogyi, Cs, Várkonyi, Á., Havass, Z., Jansen, K. P., Wolf, B.

“…From 1989 to 2001, 1 336 145 newborns were screened for biotinidase deficiency in Hungary. Fifty‐eight children with the disorder were identified as…”
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Neonatal screening for biotinidase deficiency in East‐Hungary by Havass, Z.

“…Summary There are two types of multiple carboxylase deficiency, the neonatal form with holocarboxylase synthetase defect and the late‐onset form with…”
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Laser aggregometer studies, ATP release and thromboxane B2 release and cAMP concentration of the platelets in nephrotic syndrome by Turi, S, Bereczki, C, Torday, C, Havass, Z

“…Platelet function was studied in 56 children with nephrotic syndrome, 33 were on oral prednisolone (P) treatment (group 1), while 23 were in early (< 6 months)…”
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Plasma factors influencing PGI2-like activity in patients with IgA nephropathy and Henoch-Schönlein purpura by TURI, S, NAGY, J, HASZON, I, HAVASS, Z, NEMETH, M, BERECZKI, C

“…Plasma factors influencing vascular PGI2-like activity (PSA) were studied in 45 patients with IgA nephropathy, 18 with Henoch-Schönlein purpura, including 8…”
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The effects of plasma from IgA nephropathy patients on vascular prostacyclin and platelet cyclic AMP production by Túri, S, Nagy, J, Torday, C, Havass, Z, Bereczky, C

“…The effects of plasma from 10 IgA nephropathy patients and from ten controls were studied on vascular prostacyclin (PGI2) production, the cyclic AMP (cAMP)…”
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The role of renal prostaglandin E as a possible modulator of cyclic AMP production in nephrotic syndrome by Túri, S, Havass, Z, Bodrogi, T

“…Urinary prostaglandin E (PGE) and cyclic AMP (cAMP) excretions were studied by radioimmunoassay in children with nephrotic syndrome and in a control…”
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Extensive bluish gray skin pigmentation and severe arthropathy. Endogenous ochronosis (alkaptonuria) by Lubics, A, Schneider, I, Sebök, B, Havass, Z

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Serum alpha-galactosidase activity in children with Duchenne-type muscular dystrophy and in gene carriers by László, A, Havass, Z

“…Serum alpha-galactosidase activity was studied in 21 control children, 15 children with Duchenne muscular dystrophy, and in 8 gene carrier mothers. In both the…”
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Ultrastructural study of peripheral lymphocytes and polymorphonuclear leukocytes in children with lysosomal enzymopathies and hyperlipoproteinemia by László, A, Karcsú, S, Havass, Z

“…On the basis of electronmicroscopic examinations of the peripheral lymphocytes and polymorphonuclear leukocytes (PMNL) in mucopolysaccharidosis of types I and…”
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Disturbances of lipoprotein and PGI2 metabolism in IgA nephropathy and Henoch-Schönlein purpura by Túri, S, Nagy, J, Haszon, I, Havass, Z, Németh, M, Bereczki, C

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Importance of myoglobinaemia for the outcome of hypoxia in neonates by Boda, D, Havass, Z, Hencz, P, Bartyik, K, Temesvári, P, Eck, E

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Changes of serum lipids and lipoproteins during haemodialysis treatment in dialysed chronic uraemic patients by László, A, Németh, M, Joó, I, Kiss, E, Havass, Z, Szenohradszki, P

“…Changes of serum lipids and lipoproteins were determined quantitatively before and after haemodialysis in chronic uraemic patients. Serum beta-lipoprotein…”
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Laser aggregometer studies, ATP release and thromboxane B2 release and cAMP concentration of the platelets in nephrotic syndrome by Turi, S., Bereczki, Cs, Torday, Cs, Havass, Z.

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Mass screening of neonates for histidinemia by Havass, Z, Tóth, E

“…The authors report on newborn mass-screening for histidinemia by Guthrie bacterium inhibition assay. 51,618 newborns were screened and 805 cases with more than…”
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Changes in calcium metabolism in children treated with anti-epileptic drugs: increased renal calcium reabsorption by Sztriha, L, Havass, Z

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The effect of erythropoietin on platelet function in uraemic children on haemodialysis by TURI, S, SOOS, J, TORDAY, C, BERECZKI, C, HAVASS, Z

“…The effect of 1-year erythropoietin (rHu-EPO) treatment on the bleeding time, platelet aggregation, ATP and thromboxane B2 (TXB2) release, cyclic AMP (cAMP)…”
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Mucopolysacchariduria in genetic dermatoses: hereditary epidermolysis bullosa, congenital ichthyosis and ectodermal dysplasia by László, A, Havass, Z

“…4 patients suffering from epidermolysis bullosa, 11 persons with genetically determined ichthyosis, as well as 3 cases of x-linked recessive ectodermal…”
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Biochemical and ultrastructural diagnostic problems in mucolipidoses by László, A, Lászik, Z, Klujber, L, Havass, Z

“…Biochemical and ultrastructural investigations were made in 2 children suffering from mucolipidosis type III. Among the lysosomal hydrolases the activity of…”
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Biochemical, clinical and genetic analysis of various aminoacidopathies (non-ketotic hyperglycemia, maple syrup urine disease, histidinemia, tyrosinemia) by László, A, Nagy, I, Szücs, L, Havass, Z, Sztriha, L, Svékus, A, Veres, E

“…The genetical types were classified according to the clinical findings and biochemical results in cases of 13 newborn/children suffering from various…”
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Plasma factors influencing PGI2-like activity in patients with IgA nephropathy and Henoch-Sch nlein purpura by T ri, S., Nagy, J., Haszon, I., Havass, Z., N meth, M., Bereczki, C.

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