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V Tasic

Showing results (21-30 of 35) with videos related to

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Hippokratia|November 24, 2011
Ceftriaxone associated urolithiasis in a child with hypercalciuriaV J Lozanovski, Z Gucev, V J Avramoski, et al.
Diabetes|August 14, 1998
Multiple molecular mechanisms of insulin receptor dysfunction in a patient with Donohue syndromeJ P Whitehead, M A Soos, R Jackson, et al.
Prilozi|January 25, 2011
Four generations in a family with neurofibromatosis 1: precocious puberty and optic nerve tumor (OPT)Z Gucev, M Krstevska-Konstantinova, V Tasic, et al.
Prilozi|August 9, 2011
Early-onset ocular ochronosis in a girl with alkaptonuria (AKU) and a novel mutation in homogentisate 1,2-dioxygenase (HGD)Z S Gucev, N Slaveska, N Laban, et al.
Prilozi|August 9, 2011
Rare diseases with renal involvement in the Republic of MacedoniaV Tasic, V J Lozanovski, D Danilovski, et al.
Balkan Journal of Medical Genetics : BJMG|August 14, 2023
Two Brothers from Macedonia with Gitelman SyndromeA Janchevska, V Tasic, O Jordanova, et al.
Prilozi|September 9, 2009
Type I Gaucher disease (GDI) in three siblings: enzyme replacement treatment (ERT) requiredZ S Gucev, V Tasic, N Pop-Jordanova, et al.
Prilozi|January 31, 2012
Hunter syndrome (Muccopolysaccharridosis Type II) in Macedonia and BulgariaZ S Gucev, V Tasic, I Sinigerska, et al.
Balkan Journal of Medical Genetics : BJMG|May 18, 2026
Beyond Living Donor Kidney Transplantation in COL4 Nephropathy - A Real-World Clinical Dilemma in Light of Current GuidelinesV Karanfilovski, Z Shterjova Markovska, A Canevska Taneska, et al.
Klinische Padiatrie|August 24, 2012
A premature termination mutation in a patient with Lowe syndrome without congenital cataracts: dropping the "O" in OCRLS M Pasternack, D Böckenhauer, M Refke, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Hippokratia|November 24, 2011
Ceftriaxone associated urolithiasis in a child with hypercalciuriaV J Lozanovski, Z Gucev, V J Avramoski, et al.
Diabetes|August 14, 1998
Multiple molecular mechanisms of insulin receptor dysfunction in a patient with Donohue syndromeJ P Whitehead, M A Soos, R Jackson, et al.
Prilozi|January 25, 2011
Four generations in a family with neurofibromatosis 1: precocious puberty and optic nerve tumor (OPT)Z Gucev, M Krstevska-Konstantinova, V Tasic, et al.
Prilozi|August 9, 2011
Early-onset ocular ochronosis in a girl with alkaptonuria (AKU) and a novel mutation in homogentisate 1,2-dioxygenase (HGD)Z S Gucev, N Slaveska, N Laban, et al.
Prilozi|August 9, 2011
Rare diseases with renal involvement in the Republic of MacedoniaV Tasic, V J Lozanovski, D Danilovski, et al.
Balkan Journal of Medical Genetics : BJMG|August 14, 2023
Two Brothers from Macedonia with Gitelman SyndromeA Janchevska, V Tasic, O Jordanova, et al.
Prilozi|September 9, 2009
Type I Gaucher disease (GDI) in three siblings: enzyme replacement treatment (ERT) requiredZ S Gucev, V Tasic, N Pop-Jordanova, et al.
Prilozi|January 31, 2012
Hunter syndrome (Muccopolysaccharridosis Type II) in Macedonia and BulgariaZ S Gucev, V Tasic, I Sinigerska, et al.
Balkan Journal of Medical Genetics : BJMG|May 18, 2026
Beyond Living Donor Kidney Transplantation in COL4 Nephropathy - A Real-World Clinical Dilemma in Light of Current GuidelinesV Karanfilovski, Z Shterjova Markovska, A Canevska Taneska, et al.
Klinische Padiatrie|August 24, 2012
A premature termination mutation in a patient with Lowe syndrome without congenital cataracts: dropping the "O" in OCRLS M Pasternack, D Böckenhauer, M Refke, et al.
Pageof 4