Pušeljić S - Search Results

1

First Reported Case of Gabriele-de Vries Syndrome with Spinal Dysraphism.

Koruga N, Pušeljić S, Babić M, Ćuk M, Cvitković Roić A, Vrtarić V, Soldo Koruga A, Rončević A, Tomac V, Rotim T, Turk T, Kretić D, Pušeljić N, Nađ R, Serdarušić I. Koruga N, et al. Among authors: puseljic s. Children (Basel). 2023 Mar 26;10(4):623. doi: 10.3390/children10040623. Children (Basel). 2023. PMID: 37189872 Free PMC article.

2

GPI-anchoring disorders and the heart: Is cardiomyopathy an overlooked feature?

Bayat A, Lindau T, Aledo-Serrano A, Gil-Nagel A, Barić I, Bartoniček D, Mateševac J, Ramadža DP, Žigman T, Pušeljić S, Dorner S, Bupp C, Devries S, Møller RS. Bayat A, et al. Among authors: puseljic s. Clin Genet. 2023 Nov;104(5):598-603. doi: 10.1111/cge.14405. Epub 2023 Jul 25. Clin Genet. 2023. PMID: 37489290

3

ASSOCIATION BETWEEN HIGH MOBILITY GROUP BOX 1 PROTEIN GENE (rs41369348) POLYMORPHISM AND IMMUNOGLOBULIN A VASCULITIS IN CHILDREN.

Batnožić Varga M, Šestan M, Wagner J, Crkvenac Gornik K, Kifer N, Frković M, Stefinovec L, Vučemilović Jurić V, Grgurić D, Pušeljić S, Jelušić M. Batnožić Varga M, et al. Among authors: puseljic s. Acta Clin Croat. 2023 Apr;62(1):25-35. doi: 10.20471/acc.2023.62.01.04. Acta Clin Croat. 2023. PMID: 38304371 Free PMC article.

4

Juvenile primary hypertension is associated with attenuated macro- and microvascular dilator function independently of body weight.

Kos M, Nađ T, Stupin A, Drenjančević I, Kolobarić N, Šušnjara P, Mihaljević Z, Damašek M, Pušeljić S, Jukić I. Kos M, et al. Among authors: puseljic s. J Hypertens. 2024 Nov 1;42(11):1906-1914. doi: 10.1097/HJH.0000000000003812. Epub 2024 Jul 4. J Hypertens. 2024. PMID: 39248093

5

Estimation of Salt Intake in Normotensive and Hypertensive Children: The Role of Body Weight.

Kos M, Nađ T, Stanojević L, Lukić M, Stupin A, Drenjančević I, Pušeljić S, Davidović Cvetko E, Mihaljević Z, Dumančić D, Jukić I. Kos M, et al. Among authors: puseljic s. Nutrients. 2023 Feb 1;15(3):736. doi: 10.3390/nu15030736. Nutrients. 2023. PMID: 36771442 Free PMC article.

6

Spectrum of genetic variants in 306 patients with non-syndromic hearing loss from Croatia.

Sansović I, Meašić AM, Bobinec A, Morožin Pohovski L, Odak L, Vulin K, Lozić B, Kero M, Huljev Frković S, Pušeljić S. Sansović I, et al. Among authors: puseljic s. Croat Med J. 2024 Jun 13;65(3):198-208. doi: 10.3325/cmj.2024.65.198. Croat Med J. 2024. PMID: 38868966 Free PMC article.

7

Severe Cranio-Cervical Stenosis in a Child with Saul-Wilson Syndrome: A Case Report.

Koruga N, Pušeljić S, Tomac V, Soldo Koruga A, Marjanac I, Biljan B, Šantić K, Lenz I, Pušeljić N. Koruga N, et al. Among authors: puseljic s. Children (Basel). 2022 Apr 8;9(4):532. doi: 10.3390/children9040532. Children (Basel). 2022. PMID: 35455576 Free PMC article.

8

Pan-european landscape of research into neurodevelopmental copy number variants: A survey by the MINDDS consortium.

Chawner SJRA, Mihaljevic M, Morrison S, Eser HY, Maillard AM, Nowakowska B; MINDDS Consortium; van den Bree MBM, Swillen A. Chawner SJRA, et al. Eur J Med Genet. 2020 Dec;63(12):104093. doi: 10.1016/j.ejmg.2020.104093. Epub 2020 Nov 5. Eur J Med Genet. 2020. PMID: 33160096 Free article.

9

Poverty and other correlates of obesity and underweight among 7-year-olds from Croatia and Montenegro.

Banjari I, Martinović M, Belojević G, Ašanin B, Kovačević ND, Kenjerić D, Miškulin M, Pantović S, Pušeljić S, Sokolić D, Buljan V, Bilić-Kirin V, Jakšić M. Banjari I, et al. Among authors: puseljic s. Public Health. 2020 May;182:64-69. doi: 10.1016/j.puhe.2020.01.017. Epub 2020 Mar 12. Public Health. 2020. PMID: 32172029

10

A novel PGAP3 mutation in a Croatian boy with brachytelephalangy and a thin corpus callosum.

Sakaguchi T, Žigman T, Petković Ramadža D, Omerza L, Pušeljić S, Ereš Hrvaćanin Z, Miyake N, Matsumoto N, Barić I. Sakaguchi T, et al. Among authors: puseljic s. Hum Genome Var. 2018 Mar 8;5:18005. doi: 10.1038/hgv.2018.5. eCollection 2018. Hum Genome Var. 2018. PMID: 29531774 Free PMC article.

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