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Genotyping of α-antitrypsin in ten Croatian families

Clinical biochemistry, 2000-07, Vol.33 (5), p.377-382

2000

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ETP021 Changes of serum lipoproteins during anticonvulsive treatment in epileptic children

European journal of paediatric neurology, 2007, Vol.11, p.119-119

2007

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Missense mutation W86R in exon 3 of the lipoprotein lipase gene in a boy with chylomicronemia

Clinica chimica acta, 2004-05, Vol.343 (1), p.179-184

2004

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Gluten enteropathy in Croatian children is primarily associated with the HLA-DR3-DQ2 haplotype

Liječnički vjesnik, 2000-11, Vol.122 (11-12), p.259

2000

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Growth disorders in children with type 1 diabetes mellitus

Collegium antropologicum, 2006-06, Vol.30 (2), p.297-304

2006

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Oral rehydration of infants with diarrhea: value of the modified World Health Organization (WHO) solution with a lower sodium content

Liječnički vjesnik, 1984-01, Vol.106 (1), p.16

1984

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The HLA-DR phenotype in Croatian children with gluten enteropathy

Liječnički vjesnik, 1998-09, Vol.120 (9), p.273

1998

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Clinical manifestation of compression of the celiac artery by the arcuate ligament of the diaphragm

Liječnički vjesnik, 1980-04, Vol.102 (4), p.189

1980

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Gallstone associated with acute pancreatitis in a child

Helvetica paediatrica acta, 1981-07, Vol.36 (3), p.255

1981

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Observations on hypertrophic pyloric stenosis during a period of twelve years (author's transl)

Liječnički vjesnik, 1977-05, Vol.99 (5), p.285

1977

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Inborn disorders of galactose metabolism: report of a case of "classical galactosemia" (author's transl)

Liječnički vjesnik, 1977-10, Vol.99 (10), p.589

1977

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Erythrocyte survival in children with chronic intermittent nonconjugated hyperbilirubinemia (Gilbert syndrome)

Liječnički vjesnik, 1987-04, Vol.109 (4-5), p.143

1987

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The one-hour d-xylose test in the postenteritic period. Its diagnostic and therapeutic significance (author's transl)

Liječnički vjesnik, 1981-02, Vol.103 (2-3), p.79

1981

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Disorders of coagulation in children with malabsorption

Liječnički vjesnik, 1986-10, Vol.108 (10), p.424

1986

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Histocompatibility (HLA) antigens in gluten enteropathy in children (author's transl)

Liječnički vjesnik, 1980-10, Vol.102 (10), p.563

1980

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Genotype versus phenotype of α1-antitrypsin in family studies

Journal of hepatology, 1998, Vol.28, p.144-144

1998

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One hour blood D-xylose tolerance test in children with malabsorption syndrome (author's transl)

Liječnički vjesnik, 1978-07, Vol.100 (7), p.448

1978

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Incidence of intrahospital infections in sideropenic anemia

Liječnički vjesnik, 1983-11, Vol.105 (11-12), p.440

1983

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Reye's syndrome associated with transient ornithine-transcarbamylase deficiency (author's transl)

Liječnički vjesnik, 1981-08, Vol.103 (8), p.332

1981

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Classical galactosemia and the Duarte variant of transferase in a family

Acta medica Iugoslavica, 1978, Vol.32 (1), p.93

1978

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Headaches During Febrile Illness as the Only Symptom of a Brain Tumor: A Case Report

Cephalalgia, 1995-10, Vol.15 (16_suppl), p.87-87

1995

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Cyclosporine Induced Biochemical Remission in Childhood Autoimmune Hepatitis

Acta clinica Croatica, 2008, Vol.47 (1), p.58

2008

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Taš-Raos-Rajman: Registratura i arhiva, Zagreb 1957. (Z. Jurčić)

Arhivski vjesnik, 1958, Vol.1 (1), p.543

Jurčić, Z

1958

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Congenital deficiency of prothrombin and stuart-prower factor

Thrombosis research, 1986, Vol.41, p.37-37

1986

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Congenital sensory neuropathy

Helvetica paediatrica acta, 1974-12, Vol.29 (6), p.555

1974

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Genotyping of α-antitrypsin in ten Croatian families

ETP021 Changes of serum lipoproteins during anticonvulsive treatment in epileptic children

Missense mutation W86R in exon 3 of the lipoprotein lipase gene in a boy with chylomicronemia

Gluten enteropathy in Croatian children is primarily associated with the HLA-DR3-DQ2 haplotype

Growth disorders in children with type 1 diabetes mellitus

Oral rehydration of infants with diarrhea: value of the modified World Health Organization (WHO) solution with a lower sodium content

The HLA-DR phenotype in Croatian children with gluten enteropathy

Clinical manifestation of compression of the celiac artery by the arcuate ligament of the diaphragm

Gallstone associated with acute pancreatitis in a child

Observations on hypertrophic pyloric stenosis during a period of twelve years (author's transl)

Inborn disorders of galactose metabolism: report of a case of "classical galactosemia" (author's transl)

Erythrocyte survival in children with chronic intermittent nonconjugated hyperbilirubinemia (Gilbert syndrome)

The one-hour d-xylose test in the postenteritic period. Its diagnostic and therapeutic significance (author's transl)

Disorders of coagulation in children with malabsorption

Histocompatibility (HLA) antigens in gluten enteropathy in children (author's transl)

Genotype versus phenotype of α1-antitrypsin in family studies

One hour blood D-xylose tolerance test in children with malabsorption syndrome (author's transl)

Incidence of intrahospital infections in sideropenic anemia

Reye's syndrome associated with transient ornithine-transcarbamylase deficiency (author's transl)

Classical galactosemia and the Duarte variant of transferase in a family

Headaches During Febrile Illness as the Only Symptom of a Brain Tumor: A Case Report

Cyclosporine Induced Biochemical Remission in Childhood Autoimmune Hepatitis

Taš-Raos-Rajman: Registratura i arhiva, Zagreb 1957. (Z. Jurčić)

Congenital deficiency of prothrombin and stuart-prower factor

Congenital sensory neuropathy

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