Barisić I - Search Results

1

Osteogenesis imperfecta--multi-systemic and life-long disease that affects whole family.

Primorac D, Anticević D, Barisić I, Hudetz D, Ivković A. Primorac D, et al. Among authors: barisic i. Coll Antropol. 2014 Jun;38(2):767-72. Coll Antropol. 2014. PMID: 25145021 Review.

2

Osteogenesis imperfecta at the beginning of bone and joint decade.

Primorac D, Rowe DW, Mottes M, Barisić I, Anticević D, Mirandola S, Gomez Lira M, Kalajzić I, Kusec V, Glorieux FH. Primorac D, et al. Among authors: barisic i. Croat Med J. 2001 Aug;42(4):393-415. Croat Med J. 2001. PMID: 11471191 Free article. Review.

3

[Hypophosphatasia: report of two affected girls with spontaneous improvement of skeletal defects].

Ligutić I, Barisić I, Anticević D, Vrdoljak J. Ligutić I, et al. Among authors: barisic i. Lijec Vjesn. 2005 Nov-Dec;127(11-12):288-92. Lijec Vjesn. 2005. PMID: 16583935 Croatian.

4

[Heterogeneity in osteogenesis imperfecta].

Zergollern L, Barisić I, Zergollern S. Zergollern L, et al. Among authors: barisic i. Acta Med Iugosl. 1988;42(2):115-31. Acta Med Iugosl. 1988. PMID: 3389192 Croatian. No abstract available.

5

Familial hemophagocytic lymphohistiocytosis in a 6-week-old male infant.

Jakovljević G, Kardum-Skelin I, Rogosić S, Culić S, Stepan J, Gagro A, Skarić I, Mikecin L, Bonevski A, Barisić I, Nakić M. Jakovljević G, et al. Among authors: barisic i. Coll Antropol. 2010 Jun;34(2):631-4. Coll Antropol. 2010. PMID: 20698142

6

Development of genetics in the world and in Croatia--forty years of the Croatian Society of Human Genetics of the Croatian Medical Association.

Zergollern-Ĉupak L, Barišić I, Moronin Pohovski L. Zergollern-Ĉupak L, et al. Among authors: barisic i. Coll Antropol. 2014 Sep;38(3):809-18. Coll Antropol. 2014. PMID: 25420360

7

[Mucolipidosis type III (case report)].

Ligutić I, Barisić I, Fumić K, Sabados M. Ligutić I, et al. Among authors: barisic i. Lijec Vjesn. 1996 Jan-Feb;118(1-2):17-20. Lijec Vjesn. 1996. PMID: 8759415 Croatian.

8

[Eleven years of registration of congenital anomalies in Croatia associated with the EUROCAT international project].

Ligutić I, Bariśić I, Kapitanović H, Beer Z, Modrusan-Mozetic Z, Capar M, Zuzek A, Stanojević M, Svel I, Hirsl-Hecej V. Ligutić I, et al. Among authors: barisic i. Lijec Vjesn. 1997 Feb;119(2):47-53. Lijec Vjesn. 1997. PMID: 9297035 Croatian.

9

Megalocornea-mental retardation syndrome: report of a new case.

Barisić I, Ligutić I, Zergollern L. Barisić I, et al. J Med Genet. 1996 Oct;33(10):882-3. doi: 10.1136/jmg.33.10.882. J Med Genet. 1996. PMID: 8933347 Free PMC article.

10

Expand Long PCR for fragile X mutation detection.

Hećimović S, Barisić I, Müller A, Petković I, Barić I, Ligutić I, Pavelić K. Hećimović S, et al. Among authors: barisic i. Clin Genet. 1997 Sep;52(3):147-54. doi: 10.1111/j.1399-0004.1997.tb02535.x. Clin Genet. 1997. PMID: 9377803

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