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Plasma levels and tissue expression of soluble TGFβrIII receptor in women with early-stage breast cancer and in healthy women: a prospective observational study

Journal of translational medicine, 2020-12, Vol.18 (1), p.478-11, Article 478

2020

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ORAI1 mutations abolishing store-operated Ca2+ entry cause anhidrotic ectodermal dysplasia with immunodeficiency

Journal of allergy and clinical immunology, 2018-10, Vol.142 (4), p.1297-1310.e11

2018

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Plasma levels and tissue expression of soluble TGF[beta]rIII receptor in women with early-stage breast cancer and in healthy women: a prospective observational study

Journal of translational medicine, 2020-12, Vol.18 (1)

2020

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Unravelling 5-oxoprolinuria (pyroglutamic aciduria) due to bi-allelic OPLAH mutations: 20 new mutations in 14 families

Molecular genetics and metabolism, 2016-09, Vol.119 (1-2), p.44-49

2016

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ORAI1 mutations abolishing store-operated Ca 2+ entry cause anhidrotic ectodermal dysplasia with immunodeficiency

Journal of allergy and clinical immunology, 2018-10, Vol.142 (4), p.1297

2018

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Glyceroluria and Neonatal Hemochromatosis

Journal of pediatric gastroenterology and nutrition, 2012-10, Vol.55 (4), p.e126-e128-e126-e128

2012

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Integrative Algorithms in the Diagnostics of Lysosomal Storage Diseases / INTEGRATIVNI ALGORITMI U DIJAGNOSTICI POREMEĆAJA U SKLADIŠTENJU LIZOZOMA

Journal of medical biochemistry, 2014-01, Vol.33 (1), p.82-87

2014

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Heterozygous Monocarboxylate Transporter 1 (MCT1, SLC16A1) Deficiency as a Cause of Recurrent Ketoacidosis

JIMD Reports, Volume 29, 2016, Vol.29, p.33-38

2016

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Growth characteristics of channel catfish ovary cells--influence of glucose and glutamine

Cytotechnology (Dordrecht), 2008-07, Vol.57 (3), p.273-278

2008

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Association of inflammatory status of patients with histopathological characteristics of colorectal tumors and perioperative transfusion requirements

Libri oncologici, 2019-01, Vol.46 (2-3), p.43-46

2019

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A path towards a cultured skin fibroblast biobank of patients with inherited errors of metabolism in Croatia

Paediatria Croatica, 2017-03, Vol.61 (1), p.26-32

2017

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Lysosomal acid lipase deficiency in children: our experience and a novel possibility of enzyme replacement therapy

Liječnički vjesnik, 2015-03, Vol.137 (3-4), p.81-87

2015

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MANJAK VITAMINA B12 U DJECE – PODCIJENJENA OPASNOST U SVJETLU NOVIH SPOZNAJA

Liječnički vjesnik, 2011-02, Vol.133 (1-2)

2011

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Vitamin B12 deficiency in children--underestimated danger in the light of new knowledge

Liječnički vjesnik, 2011-01, Vol.133 (1-2), p.39-50

2011

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Congenital disorders of glycosylation and project "Euroglycanet"

Liječnički vjesnik, 2007-08, Vol.129 (8-9), p.286

2007

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Laboratory diagnostics of emergency conditions associated with inborn errors of metabolism

Signa vitae, 2014-06, Vol.9 (Suppl. 1), p.70

2014

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Paediatria Croatica

Paediatria Croatica, 2013-12, Vol.57 (4), p.344-349

2013

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MANJAK LIZOSOMSKE KISELE LIPAZE U DJECE: VLASTITA ISKUSTVA I NOVA MOGUĆNOST ENZIMSKOGA NADOMJESNOG LIJEČENJA

Liječnički vjesnik, 2015-05, Vol.137 (3-4)

2015

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Acne vulgaris: myths and misconceptions among patients and family physicians

Patient education and counseling, 2004-07, Vol.54 (1), p.21-25

2004

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Biliary brush cytology for the diagnosis of malignancy: a single center experience

Collegium antropologicum, 2010-03, Vol.34 (1), p.139-143

2010

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Biliary Brush Cytology for the Diagnosis of Malignancy: A Single Center Experience

Collegium antropologicum, 2010-03, Vol.34 (1), p.139

2010

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Plasma levels and tissue expression of soluble TGFβrIII receptor in women with early-stage breast cancer and in healthy women: a prospective observational study

ORAI1 mutations abolishing store-operated Ca2+ entry cause anhidrotic ectodermal dysplasia with immunodeficiency

Plasma levels and tissue expression of soluble TGF[beta]rIII receptor in women with early-stage breast cancer and in healthy women: a prospective observational study

Unravelling 5-oxoprolinuria (pyroglutamic aciduria) due to bi-allelic OPLAH mutations: 20 new mutations in 14 families

ORAI1 mutations abolishing store-operated Ca 2+ entry cause anhidrotic ectodermal dysplasia with immunodeficiency

Glyceroluria and Neonatal Hemochromatosis

Integrative Algorithms in the Diagnostics of Lysosomal Storage Diseases / INTEGRATIVNI ALGORITMI U DIJAGNOSTICI POREMEĆAJA U SKLADIŠTENJU LIZOZOMA

Heterozygous Monocarboxylate Transporter 1 (MCT1, SLC16A1) Deficiency as a Cause of Recurrent Ketoacidosis

Growth characteristics of channel catfish ovary cells--influence of glucose and glutamine

Association of inflammatory status of patients with histopathological characteristics of colorectal tumors and perioperative transfusion requirements

A path towards a cultured skin fibroblast biobank of patients with inherited errors of metabolism in Croatia

Lysosomal acid lipase deficiency in children: our experience and a novel possibility of enzyme replacement therapy

MANJAK VITAMINA B12 U DJECE – PODCIJENJENA OPASNOST U SVJETLU NOVIH SPOZNAJA

Vitamin B12 deficiency in children--underestimated danger in the light of new knowledge

Congenital disorders of glycosylation and project "Euroglycanet"

Laboratory diagnostics of emergency conditions associated with inborn errors of metabolism

Paediatria Croatica

MANJAK LIZOSOMSKE KISELE LIPAZE U DJECE: VLASTITA ISKUSTVA I NOVA MOGUĆNOST ENZIMSKOGA NADOMJESNOG LIJEČENJA

Acne vulgaris: myths and misconceptions among patients and family physicians

Biliary brush cytology for the diagnosis of malignancy: a single center experience

Biliary Brush Cytology for the Diagnosis of Malignancy: A Single Center Experience

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