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Hippokratia
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November 24, 2011
Ceftriaxone associated urolithiasis in a child with hypercalciuria
V 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 syndrome
J 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 Macedonia
V Tasic, V J Lozanovski, D Danilovski, et al.
Balkan Journal of Medical Genetics : BJMG
|
August 14, 2023
Two Brothers from Macedonia with Gitelman Syndrome
A Janchevska, V Tasic, O Jordanova, et al.
Prilozi
|
September 9, 2009
Type I Gaucher disease (GDI) in three siblings: enzyme replacement treatment (ERT) required
Z S Gucev, V Tasic, N Pop-Jordanova, et al.
Prilozi
|
January 31, 2012
Hunter syndrome (Muccopolysaccharridosis Type II) in Macedonia and Bulgaria
Z 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 Guidelines
V 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 OCRL
S M Pasternack, D Böckenhauer, M Refke, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 35) with videos related to
Sort By:
Page
of 4
Hippokratia
|
November 24, 2011
Ceftriaxone associated urolithiasis in a child with hypercalciuria
V 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 syndrome
J 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 Macedonia
V Tasic, V J Lozanovski, D Danilovski, et al.
Balkan Journal of Medical Genetics : BJMG
|
August 14, 2023
Two Brothers from Macedonia with Gitelman Syndrome
A Janchevska, V Tasic, O Jordanova, et al.
Prilozi
|
September 9, 2009
Type I Gaucher disease (GDI) in three siblings: enzyme replacement treatment (ERT) required
Z S Gucev, V Tasic, N Pop-Jordanova, et al.
Prilozi
|
January 31, 2012
Hunter syndrome (Muccopolysaccharridosis Type II) in Macedonia and Bulgaria
Z 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 Guidelines
V 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 OCRL
S M Pasternack, D Böckenhauer, M Refke, et al.
Page
of 4