Search Results - "TASIC, VELIBOR"

IN MEMORIAM: ACADEMIC MOMIR POLENAKOVIC, PEDIATRIC NEPHROLOGY, RARE DISEASES AND PUBLISHING IN MACEDONIA.

Authors: Tasic, Velibor Gucev, Zoran

Source: Contributions / Prilozi (1857-9345). Oct2021, Vol. 42 Issue 2, p27-29. 3p.

A 4-YEAR-OLD BOY WITH BECKWITH WIEDEMANN SYNDROME (BWS).

Alternate Title: ЧЕТИРИГОДИШНО МОМЧЕ СО БЕКВИТ ВИДЕМАН СИНДРОМ (БВС)

Authors: Janchevska, Aleksandra Tasic, Velibor Laban, Nevenka et al.

Source: Contributions / Prilozi (1857-9345). Dec2018, Vol. 39 Issue 2/3, p131-135. 5p.

OBESITY IN CHILDHOOD AND ADOLESCENCE, GENETIC FACTORS.

Alternate Title: ОБЕЗНОСТА ВО ДЕТСТВОТО И АДОЛЕСЦЕНЦИЈАТА, ГЕНЕТСКИ ФАКТОРИ

Authors: Kostovski, Marko Tasic, Velibor Laban, Nevena et al.

Source: Contributions / Prilozi (1857-9345). Dec2017, Vol. 38 Issue 3, p121-133. 13p.

THE 6^TH RARE DISEASE SOUTH EASTERN EUROPE (SEE) MEETING, SKOPJE, MACEDONIA (NOVEMBER 11^TH, 2017).

Alternate Title: ШЕСТИ СОСТАНОК ЗА РЕТКИ БОЛЕСТИ НА ЈУГОИСТОЧНА ЕВРОПА, СКОПЈЕ, МАКЕДОНИЈА (11 НОЕМВРИ 2017 ГОДИНА)

Authors: Gucev, Zoran Tasic, Velibor Polenakovic, Momir

Source: Contributions / Prilozi (1857-9345). Dec2017, Vol. 38 Issue 3, p163-168. 6p.

RARE RENAL DISEASE IN MACEDONIA -- АN UPDATE.

Alternate Title: РЕТКИ БУБРЕЖНИ ЗАБОЛУВАЊА ВО МАКЕДОНИЈА – НОВИ СОЗНАНИЈА

Authors: Tasic, Velibor Gucev, Zoran Polenakovic, Momir

Source: Contributions / Prilozi (1857-9345). Dec2017, Vol. 38 Issue 3, p63-69. 7p.

A prevalent MOCS2 variant in the Roma population is associated with a novel mild form of molybdenum cofactor deficiency.

Authors: Cho, Sung Kweon Schwarz, Guenter Tasic, Velibor et al.

Source: European Journal of Pediatrics. Aug2025, Vol. 184 Issue 8, p1-13. 13p.

Recessive CHRM5 variant as a potential cause of neurogenic bladder.

Authors: Schneider, Sophia Schierbaum, Luca Burger, Wessel A. C. et al.

Source: American Journal of Medical Genetics. Part A; Aug2023, Vol. 191 Issue 8, p2083-2091, 9p

CHRONIC KIDNEY DISEASE - PEDIATRIC RISK FACTORS.

Alternate Title: ХРОНИЧНА БУБРЕЖНА БОЛЕСТ – ПЕДИЈАТРИСКИ РИЗИК-ФАКТОРИ

Authors: Tasic, Velibor Janchevska, Aleksandra Emini, Nora et al.

Source: Contributions / Prilozi (1857-9345). 2016, Vol. 37 Issue 1, p9-13. 5p.

VITAMIN D SUPPLEMENTS -- BENEFITS AND RISKS.

Authors: Tasic, Velibor Gucev, Zoran

Source: Facta Universitatis, Series: Medicine & Biology. 2016, Vol. 18 Issue 1, p1-5. 5p.

Steroid Resistant Nephrotic Syndrome-Genetic Consideration.

Authors: Tasic, Velibor Gucev, Zoran Polenakovic, Momir

Source: Contributions / Prilozi (1857-9345). Dec2015, Vol. 36 Issue 3, p5-12. 8p.

4^th Rare Disease South Eastern Europe (See) Meeting Skopje, Macedonia (November 14^th, 2015).

Authors: Gucev, Zoran Tasic, Velibor Polenakovic, Momir

Source: Contributions / Prilozi (1857-9345). Dec2015, Vol. 36 Issue 3, p154-159. 6p.

Poststreptococcal glomerulonephritis in children with congenital anomalies of the kidney and urinary tract.

Authors: Tasic, Velibor Ristoska-Bojkovska, Nadica Gucev, Zoran et al.

Source: Renal Failure. Oct2015, Vol. 37 Issue 9, p1440-1443. 4p. 3 Black and White Photographs, 1 Chart.

A truncating NRIP1 variant in an Arabic family with congenital anomalies of the kidneys and urinary tract.

Authors: Zheng, Bixia Wang, Chunyan Seltzsam, Steve et al.

Source: American Journal of Medical Genetics. Part A; Jan2022, Vol. 188 Issue 1, p310-313, 4p

Tricho-rhino-phalangeal syndrome in a 13-year-old girl with chronic renal failure and severe growth retardation.

Authors: Tasic, Velibor Gucev, Zoran Ristoska-Bojkovska, Nadica et al.

Source: Renal Failure. May2014, Vol. 36 Issue 4, p619-622. 4p.

MUTATIONAL ANALYSIS OF TAC AND TACR3 IN IDIOPATHIC CENTRAL PRECOCIOUS PUBERTY.

Authors: Krstevska-Konstantinova, Marina Tasic, Velibor B. Ribeiro Montenegro, Luciana et al.

Source: Contributions / Prilozi (1857-9345). 2014, Vol. 35 Issue 1, p129-132. 4p.

SIX WEEK FOLLOW-UP OF METABOLIC EFFECTS INDUCED BY A HIGH-FAT DIET AND STREPTOZOTOCIN IN A RODENT MODEL OF TYPE 2 DIABETES MELLITUS.

Authors: Atanasovska, Emilija Tasic, Velibor Slaninka-Miceska, Maja et al.

Source: Contributions / Prilozi (1857-9345). 2014, Vol. 35 Issue 1, p169-179. 11p.

OBESITY IN CHILDHOOD AND ADOLESCENCE, GENETIC FACTORS.

Authors: Memedi, Rexhep Tasic, Velibor Nikolic, Erieta et al.

Source: Contributions of Macedonian Academy of Sciences & Arts. 2013, Vol. 34 Issue 2, p85-89. 5p.

IDENTICAL MONOCHORIONIC TWINS WITH DOWN SYNDROME AND PATERNAL ORIGIN OF THE EXTRA CHROMOSOME 21.

Alternate Title: ИДЕНТИЧНИ МОНОХОРИОНСКИ БЛИЗНАЦИ СО ДАУНОВ СИНДРОМ И РОДИТЕЛСКО ПОТЕКЛО НА ЕКСТРАХРОМОЈОМОТ 21

Authors: Urumova A. Tasic, Velibor Bojadjieva E. et al.

Source: Contributions of Macedonian Academy of Sciences & Arts. 2012, Vol. 33 Issue 2, p41-46. 6p.

Clinical and Functional Characterization of URAT1 Variants.

Authors: Tasic, Velibor Hynes, Ann Marie Kitamura, Kenichiro et al.

Source: PLoS ONE. 2011, Vol. 6 Issue 12, p1-8. 8p.

Clinical and laboratory features of Macedonian children with OCRL mutations.

Authors: Tasic, Velibor Lozanovski, Vladimir Korneti, Petar et al.

Source: Pediatric Nephrology. Apr2011, Vol. 26 Issue 4, p557-562. 6p. 1 Black and White Photograph, 1 Chart.