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1

A 17-month-old boy with bowed legs

Ivo Baric, Veselin Škrabic, Davor Begovic, Vladimir Sarnavka, Andrea Superti-Furga

Journal:

European Journal of Pediatrics

Year:

2000

Language:

english

File:

PDF, 67 KB

english, 2000

2

Molecular basis and clinical presentation of classic galactosemia in a Croatian population

Ramadža, Danijela Petković, Sarnavka, Vladimir, Vuković, Jurica, Fumić, Ksenija, Krželj, Vjekoslav, Lozić, Bernarda, Pušeljić, Silvija, Pereira, Hana, Silva, Maria João, Tavares de Almeida, Isabel, Ba

Journal:

Journal of Pediatric Endocrinology and Metabolism

Year:

2017

Language:

english

File:

PDF, 105 KB

english, 2017

3

The molecular basis of phenylalanine hydroxylase deficiency in Croatia

Johannes Zschocke, Astrid Preusse, Vladimir Sarnavka, Ksenija Fumic, Duško Mardešic, Georg F. Hoffmann, Ivo Baric

Journal:

Year:

2003

Language:

english

File:

PDF, 47 KB

english, 2003

4

Croatian Feminists Stave Off Onslaught Of Sexist Media

sanja sarnavka, kristina mihalec and nevenka sudar

Journal:

Year:

2002

Language:

english

File:

PDF, 1.48 MB

english, 2002

5

Adrenocorticotropic hormone insensitivity associated with autonomic nervous system disorders

M. Dumić, A. Radica, Z. Sabol, V. Plavšić, Lj Brkljačić, V. Sarnavka, J. Vuković

Journal:

European Journal of Pediatrics

Year:

1991

Language:

english

File:

PDF, 342 KB

english, 1991

6

Immunological aspects of progeria (Hutchinson-Gilford syndrome) in a 15-month-old child

M. Harjaček, D. Batinić, V. Sarnavka, B. Užarević, D. Mardešić, M. Marušić

Journal:

European Journal of Pediatrics

Year:

1990

Language:

english

File:

PDF, 326 KB

english, 1990

7

S-Adenosylhomocysteine hydrolase deficiency: A second patient, the younger brother of the index patient, and outcomes during therapy

I. Barić, M. Ćuk, K. Fumić, O. Vugrek, R. H. Allen, B. Glenn, M. Maradin, L. Pažanin, I. Pogribny, M. Radoš, V. Sarnavka, A. Schulze, S. Stabler, C. Wagner, S. H. Zeisel, S. H. Mudd

Journal:

Journal of Inherited Metabolic Disease

Year:

2005

Language:

english

File:

PDF, 404 KB

english, 2005

8

Fumaric aciduria: Mild phenotype in a 8-year-old girl with novel mutations

M. Maradin, K. Fumić, H. Hansikova, M. Tesarova, L. Wenchich, S. Dorner, V. Sarnavka, J. Zeman, I. Barić

Journal:

Journal of Inherited Metabolic Disease

Year:

2006

Language:

english

File:

PDF, 137 KB

english, 2006

9

A new case of succinyl-CoA:acetoacetate transferase deficiency: Favourable course despite very low residual activity

I. Barić, V. Sarnavka, K. Fumić, M. Maradin, D. Begović, J.P.N. Ruiter, R.J.A. Wanders

Journal:

Journal of Inherited Metabolic Disease

Year:

2001

Language:

english

File:

PDF, 36 KB

english, 2001

10

3FC1.6 S-adenosylhomocysteine hydrolase deficiency -a natural model for study of various neurological problems in children with possible dysmethylation pathogenesis

I. Barić, M. Ćuk, D. Petković Ramadža, K. Bilić, I. Martinac, V. Sarnavka, O. Vugrek, H.S. Mudd, K. Fumić

Journal:

European Journal of Paediatric Neurology

Year:

2011

Language:

english

File:

PDF, 38 KB

english, 2011

11

P05.10 Early-onset Gaucher disease (GD) in an infant – what phenotype to expect along the neuronopathic continuum and how to treat it?

M. Ćuk, K. Fumić, K. Bilić, E. Sidransky, A. Vellodi, K. Juras, V. Sarnavka, L. Jelinić, L.J. Rajić, M. Mikulić, R. Stern Padovan, M. Čačić Hribljan, T. Matić, M. Cvitković, S. Galić, M. Novak, D. Ric

Journal:

European Journal of Paediatric Neurology

Year:

2011

Language:

english

File:

PDF, 54 KB

english, 2011

12

The Role of Plasma Exchange in the Treatment of Severe Forms of Hemolytic-Uremic Syndrome in Childhood

Jasna Slaviček, Zvonimir Puretić, Milivoj Novak, Vladimir Sarnavka, Vesna Benjak, Snežana Glavaš-Boras, Sigmund Thune

Journal:

Artificial Organs

Year:

1995

Language:

english

File:

PDF, 463 KB

english, 1995

13

Genotype-predicted tetrahydrobiopterin (BH4)-responsiveness and molecular genetics in Croatian patients with phenylalanine hydroxylase (PAH) deficiency

Iva Karačić, David Meili, Vladimir Sarnavka, Caroline Heintz, Beat Thöny, Danijela Petković Ramadža, Ksenija Fumić, Duško Mardešić, Ivo Barić, Nenad Blau

Journal:

Molecular Genetics and Metabolism

Year:

2009

Language:

english

File:

PDF, 212 KB

english, 2009

14

Osteomyelitis as a complication of capillary blood collection for neonatal screening

Gjurić, G., Nikolić, E., Benjak, V., Mardešić, D., Sarnavka, V.

Journal:

Year:

1992

Language:

english

File:

PDF, 301 KB

english, 1992

15

Corticosterone methyloxydase deficiency type II in a Croatian girl

Dr. D. Mardešić,V. Sarnavka,M. Dumić…

Journal:

Journal of Endocrinological Investigation

Year:

1992

Language:

english

File:

PDF, 494 KB

english, 1992

16

Using the master's tools: feminism, media and ending violence against women

Sarnavka, Sanya

Journal:

Gender & Development

Year:

2003

Language:

english

File:

PDF, 545 KB

english, 2003

17

Molecular Analysis and Electromyoneurographic Abnormalities in Croatian Children with Proximal Spinal Muscular Atrophies

Barišić, Nina, Sertić, Jadranka, Billi, Christopher, Barić, Ivo, Sarnavka, Vladimir, Babić, Tomislav, Hrabač, Pero, Begović, Davor, Florentin, Lina, Stavljenić-Rukavina, Ana

Journal:

Clinical Chemistry and Laboratory Medicine

Year:

1998

Language:

english

File:

PDF, 33 KB

english, 1998

18

S-adenosylhomocysteine hydrolase deficiency in a human: A genetic disorder of methionine metabolism

Baric, I., Fumic, K., Glenn, B., Cuk, M., Schulze, A., Finkelstein, J. D., James, S. J., Mejaski-Bosnjak, V., Pazanin, L., Pogribny, I. P., Rados, M., Sarnavka, V., Scukanec-Spoljar, M., Allen, R. H.,

Journal:

Proceedings of the National Academy of Sciences

Year:

2004

Language:

english

File:

PDF, 374 KB

english, 2004

19

POMT1-Associated Walker-Warburg Syndrome: A Disorder of Dendritic Development of Neocortical Neurons

Judaš, M., Sedmak, G., Radoš, M., Sarnavka, V., Fumić, K., Willer, T., Gross, C., Hehr, U., Strahl, S., Ćuk, M., Barić, I.

Journal:

Neuropediatrics

Year:

2009

Language:

english

File:

PDF, 988 KB

english, 2009

20

Women Reinventing Globalisation || Using the Master's Tools: Feminism, Media and Ending Violence against Women

Journal:

Gender & Development

Year:

2003

Language:

english

File:

PDF, 199 KB

english, 2003

21

Hyperinsulinism-hyperammonemia syndrome: a de novo mutation of the GLUD1 gene in twins and a review of the literature

Ninković, Dorotea, Sarnavka, Vladimir, Bašnec, Anica, Ćuk, Mario, Ramadža, Danijela Petković, Fumić, Ksenija, Kušec, Vesna, Santer, René, Barić, Ivo

Journal:

Journal of Pediatric Endocrinology and Metabolism

Year:

2016

Language:

english

File:

PDF, 166 KB

english, 2016