Velibor Tasic

Velibor Tasic

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Velibor Tasic

Publications by authors named "Velibor Tasic"

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Tissue-specific mosaicism in a patient with Rubinstein-Taybi syndrome and CREBBP exon 1 duplication.

Clin Dysmorphol 2019 Jul;28(3):142-144

Institute of Human Genetics, University Medical Centre of the Johannes Gutenberg University, Mainz, Mainz, Germany.

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http://dx.doi.org/10.1097/MCD.0000000000000268DOI Listing
July 2019

Severe digital malformations in a rare variant of fibrodysplasia ossificans progressiva.

Am J Med Genet A 2019 Jul 22;179(7):1310-1314. Epub 2019 Apr 22.

Department of Orthopaedic Surgery, Center for Research in FOP & Related Disorders, Perelman School of Medicine, The University of Pennsylvania, Philadelphia, Pennsylvania.

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http://dx.doi.org/10.1002/ajmg.a.61153DOI Listing
July 2019

Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract.

Nat Genet 2019 04;51(4):764

Division of Nephrology, Department of Medicine, Columbia University, New York, NY, USA.

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http://dx.doi.org/10.1038/s41588-019-0376-0DOI Listing
April 2019

Incidental Detection of Dent-2 Disease in an Infant with Febrile Proteinuria.

Med Princ Pract 2018 17;27(4):392-395. Epub 2018 May 17.

University Children's Hospital, Medical School Skopje, Skopje, Macedonia.

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http://dx.doi.org/10.1159/000490147DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6167689PMC
January 2019

The copy number variation landscape of congenital anomalies of the kidney and urinary tract.

Nat Genet 2019 01 21;51(1):117-127. Epub 2018 Dec 21.

Division of Nephrology, Department of Medicine, Columbia University, New York, NY, USA.

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http://www.nature.com/articles/s41588-018-0281-y
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http://dx.doi.org/10.1038/s41588-018-0281-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6668343PMC
January 2019

A 4-Year-Old Boy with Beckwith Wiedemann Syndrome (BWS).

Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2018 Dec;39(2-3):131-135

Center for Human Genetics, Bioscientia Institute for Medical Diagnostics Ingelheim, Germany.

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http://dx.doi.org/10.2478/prilozi-2018-0052DOI Listing
December 2018

Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.

J Am Soc Nephrol 2018 09 24;29(9):2348-2361. Epub 2018 Aug 24.

Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts;

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http://www.jasn.org/lookup/doi/10.1681/ASN.2017121265
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http://dx.doi.org/10.1681/ASN.2017121265DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6115658PMC
September 2018

Non Catether Induced Renal and Inferior Vena Cava Trombosis in a Neonate: A Case Report.

Open Access Maced J Med Sci 2018 Sep 23;6(9):1678-1681. Epub 2018 Aug 23.

Nephrology Department, University Children Hospital, Skopje, Republic of Macedonia.

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http://dx.doi.org/10.3889/oamjms.2018.306DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182507PMC
September 2018

Growth Hormone Treatment in Children Born Small for Gestational Age (SGA).

Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2018 Jul;39(1):143-149

University Children's Hospital, Medical Faculty Skopje, Republic of Macedonia.

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http://dx.doi.org/10.2478/prilozi-2018-0034DOI Listing
July 2018

Parameters of Metabolic Syndrome in Obese Children and Adolescents.

Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2018 Jul;39(1):105-114

Macedonian Academy of Science and Arts, Skopje, Republic of Macedonia.

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http://dx.doi.org/10.2478/prilozi-2018-0030DOI Listing
July 2018

Low Molecular Weight Proteinuria in Children with Distal Renal Tubular Acidosis.

Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2018 Jul;39(1):91-95

University Children's Hospital, Medical School Skopje, Republic of Macedonia.

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http://dx.doi.org/10.2478/prilozi-2018-0028DOI Listing
July 2018

Homeostasis Model Assessment - Insulin Resistance and Sensitivity (HOMA-IR and IS) Index in Overweight Children Born Small for Gestational Age (SGA).

Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2018 Jul;39(1):83-89

Macedonian Academy of Siences and Arts, Skopje, Republic of Macedonia.

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http://dx.doi.org/10.2478/prilozi-2018-0027DOI Listing
July 2018

The Spectrum of Kidney Diseases in Children Associated with Low Molecular Weight Proteinuria.

Open Access Maced J Med Sci 2018 May 16;6(5):814-819. Epub 2018 May 16.

University Children's Hospital, Medical Faculty, Ss Cyril and Methodius University of Skopje, Skopje, Republic of Macedonia.

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http://dx.doi.org/10.3889/oamjms.2018.221DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5985860PMC
May 2018

Gene Alterations in Small for Gestational Age (SGA) Children.

Open Access Maced J Med Sci 2018 May 13;6(5):790-793. Epub 2018 Jun 13.

University Children's Hospital, Faculty of Medicine, Ss Cyril and Methodius University of Skopje, Skopje, Republic of Macedonia.

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http://dx.doi.org/10.3889/oamjms.2018.209DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5985885PMC
May 2018

Metabolic Profiles in Obese Children and Adolescents with Insulin Resistance.

Open Access Maced J Med Sci 2018 Mar 14;6(3):511-518. Epub 2018 Mar 14.

University Clinic of Child Diseases, Faculty of Medicine, Ss Cyril and Methodius University of Skopje, Skopje, Republic of Macedonia.

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http://dx.doi.org/10.3889/oamjms.2018.097DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5874375PMC
March 2018

Obesity in Childhood and Adolescence, Genetic Factors.

Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2017 Dec;38(3):121-133

Faculty of Medicine, University "Ss. Cyril and Methodius", 50 Divizija BB,1000 Skopje, Republic of Macedonia.

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http://dx.doi.org/10.2478/prilozi-2018-0013DOI Listing
December 2017

Rare Renal Disease in Macedonia - An Update.

Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2017 Dec;38(3):63-69

Macedonia Academy of Science and Arts, Skopje, Republic of Macedonia.

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http://dx.doi.org/10.2478/prilozi-2018-0007DOI Listing
December 2017

The 6th Rare Disease South Eastern Europe (See) Meeting, Skopje, Macedonia (November 11th, 2017).

Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2017 Dec;38(3):163-168

Macedonian Academy of Science and Arts, Skopje, Republic of Macedonia.

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http://dx.doi.org/10.2478/prilozi-2018-0018DOI Listing
December 2017

Kidney diseases in children - early diagnosis and prevention.

Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2016;37(1):5-7

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http://dx.doi.org/10.1515/prilozi-2016-0009DOI Listing
June 2017

Chronic kidney disease - pediatric risk factors.

Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2016;37(1):9-13

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http://dx.doi.org/10.1515/prilozi-2016-0003DOI Listing
June 2017

5th Rare Disease South Eastern Europe (SEE) Meeting, Skopje, Macedonia (November 15th, 2016).

Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2017 Mar;38(1):119-123

Macedonian Academy of Sciences and Arts, Bul. Krste Misirkov, No. 2, Skopje.

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http://dx.doi.org/10.1515/prilozi-2017-0016DOI Listing
March 2017

Congenital Anomalies of the Kidney and Urinary Tract in Children Born Small for Gestational Age.

Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2017 Mar;38(1):53-57

University Children's Hospital Skopje, Medical Faculty Skopje.

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http://dx.doi.org/10.1515/prilozi-2017-0007DOI Listing
March 2017

Genetic Drivers of Kidney Defects in the DiGeorge Syndrome.

N Engl J Med 2017 02 25;376(8):742-754. Epub 2017 Jan 25.

From the Division of Nephrology (E.L.-R., M.V., V.P.C., Z.Y., A.M., J.M., N.J.S., D.A.F., R.D., M.W., G.S.M., M.B., J.M.B., K.K., A.G.G., S.S.-C.) and the Division of Nephrology in Medicine and Zuckerman Mind Brain Behavior Institute (B.H.), the Departments of Systems Biology (D.S.P., B.H.), Biochemistry and Molecular Biophysics (B.H.), and Pathology (V.D.), and the Howard Hughes Medical Institute (D.S.P., B.H.), Columbia University, and the Department of Genetics and Development, Columbia University Medical Center (Q.L., V.E.P.), New York, and the Department of Genetics, Albert Einstein College of Medicine, Bronx (S.E.R., B.E.M.) - all in New York; the Center for Human Disease Modeling, Duke University, Durham, NC (Y.P.L., B.R.A., N. Katsanis); the Departments of Internal Medicine-Nephrology (E.A.O.) and Pediatrics-Nephrology (M.G.S., C.E.G., V.V.-W.), University of Michigan School of Medicine, Ann Arbor; the Department of Anatomy, Histology, and Embryology, School of Medicine, University of Split (K.V., M.S.-B.), and the Departments of Pediatrics (A.A., M. Saraga) and Pathology (N. Kunac), University Hospital of Split, Split, Croatia; the Department of Pediatric Nephrology, VU University Medical Center, Amsterdam (R.W., J.A.E.W.); the Department of Medicine, Boston Children's Hospital (A.V., F.H.), and Harvard Medical School, Boston (A.V., F.H., I.A.D.), and the Nephrology Division, Massachusetts General Hospital, Charlestown (I.A.D.) - all in Massachusetts; the Division of Nephrology, Dialysis, Transplantation, and Laboratory on Pathophysiology of Uremia, Istituto G. Gaslini, Genoa (M.B., A.C., G.M.G.), the Department of Clinical and Experimental Medicine, University of Parma (M.B., M. Maiorana, L.A.), and the Pediatric Surgery Unit, University Hospital of Parma (E.C.), Parma, the Section of Nephrology, Department of Emergency and Organ Transplantation, University of Bari, Bari (L.G.), the Department of Medical Sciences, University of Milano, and Institute of Biomedical Technologies, Italian National Institute of Research ITB-CNR, Milan (D.C.), and Dipartimento Ostetrico-Ginecologico e Seconda Divisione di Nefrologia ASST Spedali Civili e Presidio di Montichiari (C.I.) and Cattedra di Nefrologia, Università di Brescia, Seconda Divisione di Nefrologia Azienda Ospedaliera Spedali Civili di Brescia Presidio di Montichiari (F.S.), Brescia - all in Italy; the Department of General and Transplant Surgery, University Hospital of Heidelberg, Germany (V.J.L.); the Department of Pediatric Nephrology, Centre de Référence des Maladies Rénales Héréditaires de l'Enfant et de l'Adulte (R.S., L.H., C.J.), INSERM UMR 1163, Laboratory of Hereditary Kidney Diseases (R.S.), Necker-Enfants Malades Hospital, Paris Descartes-Sorbonne Paris Cite University, Imagine Institute (R.S.), Sorbonne Universités, UPMC 06, Plateforme Post-génomique de la Pitié-Salpêtrière, UMS 2 Omique, Inserm US029 (W.C.), Paris, and the Department of Genetics, Centre Hospitalier Universitaire de Reims, Unité de Formation et de Recherche de Médecine, Reims (D.G.) - both in France; the Department of Neurology, University of Washington School of Medicine, and Northwest VA Parkinson's Disease Research, Education and Clinical Centers, Seattle (A. Samii); the Division of Human Genetics, Department of Pediatrics, 22q and You Center, Children's Hospital of Philadelphia and Perelman School of Medicine at the University of Pennsylvania (D.M.M.-M., T.B.C., E.H.Z., S.L.F.), Division of Nephrology, Children's Hospital of Philadelphia (S.L.F.), and the Department of Genetics, University of Pennsylvania (H.H.), Philadelphia; the Dialysis Unit, Jagiellonian University Medical College (D.D.), and the Department of Pediatric Nephrology, Jagiellonian University Medical College (M. Miklaszewska), Krakow, the Department of Pediatrics, Immunology and Nephrology, Polish Mother's Memorial Hospital Research Institute, Lodz (M.T.), the Department of Pediatric Nephrology Medical University of Lublin, Lublin (P.S.), the Department of Pediatrics, School of Medicine with the Division of Dentistry in Zabrze, Medical University of Silesia, Katowice (M. Szczepanska), the Department of Pediatrics and Nephrology, Medical University of Warsaw, Warsaw (M.M.-W., G.K., A. Szmigielska), and Krysiewicza Children's Hospital (M.Z.) and the Department of Medical Genetics, Poznan University of Medical Sciences, and Center for Medical Genetics GENESIS (A.L.-B., A.M.-K.), Poznań - all in Poland; the Department of Clinical Genetics (J.M.D., D.B.), National Children's Research Centre (J.M.D., P.P.), and University College Dublin School of Medicine (D.B.), Our Lady's Children's Hospital Crumlin, and the National Children's Hospital Tallaght (P.P.), Dublin, Ireland; the Division of Pediatric Nephrology, Children's Mercy Hospital, Kansas City, MO (B.A.W.); University Children's Hospital, Medical Faculty of Skopje, Skopje, Macedonia (Z.G., V.T.); Faculty of Medicine, Palacky University, Olomouc, Czech Republic (H.F.); the Division of Pediatric Nephrology, University of New Mexico Children's Hospital, Albuquerque (C.S.W.); Ben May Department for Cancer Research, University of Chicago, Chicago (A.I.); and the Department of Genetics, Howard Hughes Medical Institute, and Yale Center for Mendelian Genomics, Yale University, New Haven, CT (R.P.L.).

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http://dx.doi.org/10.1056/NEJMoa1609009DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559731PMC
February 2017

The Child Health Care System of Macedonia.

J Pediatr 2016 10 22;177S:S127-S137. Epub 2016 Sep 22.

University Children's Hospital, Medical School, Skopje, Macedonia.

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http://dx.doi.org/10.1016/j.jpeds.2016.04.049DOI Listing
October 2016

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

Ren Fail 2015 3;37(9):1440-3. Epub 2015 Sep 3.

b Department of General and Transplant Surgery , University Hospital Heidelberg , Heidelberg , Germany.

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http://dx.doi.org/10.3109/0886022X.2015.1074488DOI Listing
August 2016

Steroid Resistant Nephrotic Syndrome-Genetic Consideration.

Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2015 ;36(3):5-12

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http://dx.doi.org/10.1515/prilozi-2015-0073DOI Listing
August 2016

Compound Galactosylceramidase Gene (GALC) Heterozygosity in a Boy with Infantile Krabbe Disease (KD).

Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2015 ;36(3):99-101

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http://dx.doi.org/10.1515/prilozi-2015-0084DOI Listing
August 2016

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

Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2015 ;36(3):151-6

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http://dx.doi.org/10.1515/prilozi-2015-0091DOI Listing
August 2016

Mutations in SLC26A1 Cause Nephrolithiasis.

Am J Hum Genet 2016 06 19;98(6):1228-1234. Epub 2016 May 19.

Division of Nephrology, Department of Medicine, Boston Children's Hospital and Harvard Medical School, Boston, MA 02115, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2016.03.026DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4908148PMC
June 2016

Identical monochorionic twins with down syndrome and paternal origin of the extra chromosome 21.

Prilozi 2012 ;33(2):41-6

Medical Faculty Skopje, 50 Divizija BB, Skopje, R. Macedonia.

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April 2016

The degree of H19 hypomethylation in children with Silver-Russel syndrome (SRS) is not associated with the severity of phenotype and the clinical severity score (CSS).

Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2013 ;34(2):79-83

Medical Faculty Skopje, 50 Divizija BB, 1000 Skopje, R. Macedonia.

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April 2016

Obesity in childhood and adolescence, genetic factors.

Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2013 ;34(2):85-9

Medical Faculty Skopje, 50 Divizija BB, 1000 Skopje, R. Macedonia.

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April 2016

Where are we now in the investigation of rare diseases in the Republic of Macedonia?

Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2014 ;35(1):85-6

Macedonian Academy of Sciences and Arts, Skopje, R. Macedonia.

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March 2016

Six week follow-up of metabolic effects induced by a high-fat diet and streptozotocin in a rodent model of type 2 diabetes mellitus.

Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2014 ;35(1):169-79

Department of Preclinical and Clinical Pharmacology with Toxicology, Medical Faculty, Vodnjanska b.b., Skopje, R. Macedonia.

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March 2016

Mutational analysis of TAC and TACR3 in idiopathic central precocious puberty.

Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2014 ;35(1):129-32

Medical Faculty, Skopje, R. Macedonia.

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March 2016

Nephrolithiasis and Nephrocalcinosis in Children - Metabolic and Genetic Factors.

Pediatr Endocrinol Rev 2015 Sep;13(1):468-76

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September 2015

Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tract.

J Am Soc Nephrol 2014 Sep 3;25(9):1917-22. Epub 2014 Apr 3.

Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts; Howard Hughes Medical Institute, Chevy Chase, Maryland

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http://dx.doi.org/10.1681/ASN.2013101103DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4147986PMC
September 2014

Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract.

Kidney Int 2014 Jun 15;85(6):1429-33. Epub 2014 Jan 15.

1] Division of Nephrology, Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA [2] Howard Hughes Medical Institute, Chevy Chase, Maryland, USA.

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http://dx.doi.org/10.1038/ki.2013.508DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4040148PMC
June 2014

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

Ren Fail 2014 May 6;36(4):619-22. Epub 2014 Feb 6.

Medical Faculty Skopje, University Children's Hospital , Skopje , Macedonia and.

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http://dx.doi.org/10.3109/0886022X.2014.882237DOI Listing
May 2014

Nephropathic cystinosis--a gap between developing and developed nations.

N Engl J Med 2014 Apr;370(14):1366-7

Centre de Référence des Maladies Rénales Rares, Bron, France

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http://dx.doi.org/10.1056/NEJMc1309480DOI Listing
April 2014

Mutations in DSTYK and dominant urinary tract malformations.

N Engl J Med 2013 Aug 17;369(7):621-9. Epub 2013 Jul 17.

Divisions of Nephrology (S.S.-C., R.V.S., N.P., K.E.B., S.N.N., B.J.P., P.L.W., M.V., F.L., R.S., N.P., N.K., K.K., Q.A.-A., A.G.G.) and Pediatric Nephrology (P.L.W.) and the Department of Pathology (V.D.D.), Columbia University, and the Department of Medicine, St. Luke's-Roosevelt Hospital Center (S.S.-C.), New York; the Department of Genetics, Howard Hughes Medical Institute, and Yale Center for Mendelian Genomics, Yale University, New Haven, CT (M.C., M.S., R.P.L.); the Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, South Korea (M.C.); the Division of Nephrology, Dialysis, and Transplantation (M.B., F.L., G.C., A.C., M.D., C.M., G.P., G.M.G.) and Laboratory of Molecular Genetics (G.S., R.R.), Istituto Giannina Gaslini, the Division of Nephrology, Department of Internal Medicine (M.B.), and Dipartimento di Neuroscienze, Riabilitazione, Oftalmologia, Genetica e Scienze Materno Infantili (R.R.), University of Genoa, and IRCCS San Martino-IST (M.B.), Genoa; Cattedra di Nefrologia, Università di Brescia, Seconda Divisione di Nefrologia Azienda Ospedaliera Spedali Civili di Brescia Presidio di Montichiari, Brescia (C.I., F.S.); the Department of Clinical Medicine, Nephrology, and Health Sciences, Unit of Nephrology, University of Parma, Parma (B.B., S.G., L.A.); the Department of Medical and Surgical Sciences, University of Foggia, Foggia (M.G.); the Department of Emergency and Organ Transplantation, University of Bari, Bari (L.G.); and the Division of Nephrology and Dialysis, Hospital of Alghero, Alghero (D.C.) - all in Italy; the Nephrology Division, Massachusetts General Hospital (Y.L., I.A.D.), and Department of Genetics, Harvard Medical School (I.A.D.), Charlestown, MA; University Children's Hospital, Medical School of Skopje, Skopje, Macedonia (V.J.L., N.R.-B., Z.G., V.T.); the Department of Medical Genetics, Poznan University of Medical Sciences, Poznan, Poland (A.M.-K., A.L.-B.); and the Department of Pediatrics, University Hospital of Split (D.K.V., M.S.), and the Department of Anatomy, Histology, and Embryology (K.V., M.S.-B.), School of Medicine (M.S.), University of Split, Split, Croatia.

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http://dx.doi.org/10.1056/NEJMoa1214479DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846391PMC
August 2013

Autosomal dominant spondylocostal dysostosis is caused by mutation in TBX6.

Hum Mol Genet 2013 Apr 17;22(8):1625-31. Epub 2013 Jan 17.

Developmental and Stem Cell Biology Division, Victor Chang Cardiac Research Institute, Sydney, NSW 2010, Australia.

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http://dx.doi.org/10.1093/hmg/ddt012DOI Listing
April 2013

Two siblings with Niemann-Pick disease (NPD) type B: clinical findings and novel mutations of the acid sphingomyelinase gene.

Indian J Pediatr 2013 Feb 25;80(2):163-4. Epub 2012 Feb 25.

Department of Endocrinology and Genetics, Pediatric Clinic, Medical Faculty Skopje, 50 Divizija BB, 1000, Skopje, Macedonia.

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http://link.springer.com/10.1007/s12098-012-0717-9
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http://dx.doi.org/10.1007/s12098-012-0717-9DOI Listing
February 2013

Molecular characterization of cystinuria in south-eastern European countries.

Urolithiasis 2013 Feb 27;41(1):21-30. Epub 2012 Dec 27.

Macedonian Academy of Science and Arts, Research Centre for Genetic Engineering and Biotechnology "Georgi D. Efremov", 1000, Skopje, Republic of Macedonia.

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http://dx.doi.org/10.1007/s00240-012-0531-xDOI Listing
February 2013

A novel GH1 mutation in a family with isolated growth hormone deficiency type II.

Horm Res Paediatr 2012 22;77(3):200-4. Epub 2011 Dec 22.

Medical Faculty Skopje, Skopje, Macedonia.

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http://dx.doi.org/10.1159/000334643DOI Listing
August 2012

Failure to thrive and nephrolithiasis in a boy with congenital cyanotic heart anomaly.

Pediatr Nephrol 2011 Dec 1;26(12):2153-7. Epub 2011 Mar 1.

Department of Pediatric Nephrology, University Children's Hospital, Medical School Skopje, 17 Vodnjanska, 1000, Skopje, Macedonia.

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http://www.biopku.org/pdf/tasic_2011_pn.pdf
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http://link.springer.com/content/pdf/10.1007%2Fs00467-011-17
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http://link.springer.com/10.1007/s00467-011-1786-0
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http://dx.doi.org/10.1007/s00467-011-1786-0DOI Listing
December 2011

Billateral polycystic kidneys in a girl with WAGR syndrome.

Indian J Pediatr 2011 Oct 10;78(10):1290-2. Epub 2011 Jun 10.

University Children´s Hospital, Medical Faculty Skopje, 50 Divizija BB, 1000 Skopje, Macedonia.

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http://dx.doi.org/10.1007/s12098-011-0457-2DOI Listing
October 2011

Clinical and laboratory features of Macedonian children with OCRL mutations.

Pediatr Nephrol 2011 Apr 20;26(4):557-62. Epub 2011 Jan 20.

University Children's Hospital, Medical School Skopje, Skopje, Macedonia.

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http://dx.doi.org/10.1007/s00467-010-1758-9DOI Listing
April 2011

Recurrent urinary tract infections in an infant with antenatal Bartter syndrome.

World J Pediatr 2011 Feb 1;7(1):86-8. Epub 2010 Feb 1.

Department of Pediatric Nephrology, University Children's Hospital, Skopje, Macedonia.

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http://dx.doi.org/10.1007/s12519-010-0021-6DOI Listing
February 2011

Nephrotic syndrome occurring during tiopronin treatment for cystinuria.

Eur J Pediatr 2011 Feb 6;170(2):247-9. Epub 2010 Oct 6.

University Children's Hospital, Medical School Skopje, 17 Vodnjanska, 1000 Skopje, Macedonia.

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http://dx.doi.org/10.1007/s00431-010-1315-3DOI Listing
February 2011

Late diagnosis of primary hyperoxaluria after failed kidney transplantation.

Int Urol Nephrol 2010 Sep 18;42(3):825-9. Epub 2009 Dec 18.

University Department of Nephrology, Medical Faculty, University of Skopje, Vodnjanska 17, 1000 Skopje, Macedonia.

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http://www.biopku.org/pdf/spasovski_2009_iun.pdf
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http://link.springer.com/10.1007/s11255-009-9690-2
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http://dx.doi.org/10.1007/s11255-009-9690-2DOI Listing
September 2010

McCune-Albright syndrome (MAS): early and extensive bone fibrous dysplasia involvement and "mistaken identity" oophorectomy.

J Pediatr Endocrinol Metab 2010 Aug;23(8):837-42

Faculty of Medicine Skopje, 50 Divizija BB, 1000 Skopje, Macedonia.

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http://dx.doi.org/10.1515/jpem.2010.135DOI Listing
August 2010

The impact of CFNS-causing EFNB1 mutations on ephrin-B1 function.

BMC Med Genet 2010 Jun 17;11:98. Epub 2010 Jun 17.

Institut für Humangenetik, Universitätsklinikum, Otto-von-Guericke-Universität, Magdeburg, Germany.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2901216PMC
June 2010

A patient with unilateral tibial aplasia and accessory scrotum: a pure coincidence or nonfortuitous association?

Case Rep Med 2010 3;2010:898636. Epub 2010 Feb 3.

University Pediatric Hospital, Division for Endocrinology and Genetics, Vodnjanska BB, 1000 Skopje, Macedonia.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2817541PMC
February 2010

Analysis of TSHZ2 and TSHZ3 genes in congenital pelvi-ureteric junction obstruction.

Nephrol Dial Transplant 2010 Jan 10;25(1):54-60. Epub 2009 Sep 10.

Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Oxford OX3 9DS, UK.

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http://dx.doi.org/10.1093/ndt/gfp453DOI Listing
January 2010

Papillorenal syndrome after Beta-interferon treatment in pregnancy.

Ren Fail 2009 ;31(7):602-5

Medical Faculty Skopje, 50 Divizija BB, 1000, Skopje, Macedonia.

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http://dx.doi.org/10.1080/08860220902968862DOI Listing
January 2010

Dent-2 disease: a mild variant of Lowe syndrome.

J Pediatr 2009 Jul;155(1):94-9

Department of Pediatrics, VU University Medical Center, Amsterdam, The Netherlands.

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July 2009