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Seroreactivity to Dirofilaria antigens in people from different areas of Serbia.
- Published in:
- 2014
- By:
- Publication type:
- journal article
Lesch-Nyhan syndrome: a novel complex mutation with severe phenotype.
- Published in:
- Clinical Genetics, 2010, v. 78, n. 3, p. 296, doi. 10.1111/j.1399-0004.2010.01428.x
- By:
- Publication type:
- Article
CLINICAL COURSE AND OUTCOME IN PATIENTS WITH EARLY DIAGNOSED CAKUT.
- Published in:
- Journal of Perinatal Medicine, 2017, v. 45, p. 322, doi. 10.1515/jpm-2017-3002
- By:
- Publication type:
- Article
Occurrence of subclinical post-streptococcal glomerulonephritis in family contacts.
- Published in:
- 2003
- By:
- Publication type:
- journal article
Measurement of Extremely Low Frequent Magnetic Induction in Residential Buildings.
- Published in:
- International Journal of Environmental Research, 2014, v. 8, n. 3, p. 583
- By:
- Publication type:
- Article
Mal'cev nilpotent algebras.
- Published in:
- Archiv der Mathematik, 1999, v. 72, n. 1, p. 22, doi. 10.1007/s000130050298
- By:
- Publication type:
- Article
OCRL1 mutation in a boy with Dent disease, mild mental retardation, but without cataracts.
- Published in:
- World Journal of Pediatrics, 2011, v. 7, n. 3, p. 280, doi. 10.1007/s12519-011-0312-6
- By:
- Publication type:
- Article
Aldosterone Synthase Deficiency Type II with Hypospadias.
- Published in:
- Indian Pediatrics, 2012, v. 49, n. 4, p. 318
- By:
- Publication type:
- Article
The effects of nimodipine on coronary flow, nitrite outflow and superoxide anion release in isolated rat heart
- Published in:
- 2003
- By:
- Publication type:
- Abstract
Ceftriaxone associated urolithiasis in a child with hypercalciuria.
- Published in:
- 2011
- By:
- Publication type:
- Case Study
Mutation analysis of the Uromodulin gene in 96 individuals with urinary tract anomalies (CAKUT)
- Published in:
- 2009
- By:
- Publication type:
- Journal Article
Nephrotic syndrome in a child after a bee sting.
- Published in:
- Pediatric Nephrology, 2000, v. 15, n. 3/4, p. 245, doi. 10.1007/s004670000452
- By:
- Publication type:
- Article
Multiple molecular mechanisms of insulin receptor dysfunction in a patient with Donohue syndrome.
- Published in:
- 1998
- By:
- Publication type:
- journal article
Factitious proteinuria in a diabetic patient.
- Published in:
- 2001
- By:
- Publication type:
- Case Study
Imaging of children with culture-negative acute pyelonephritis.
- Published in:
- 2003
- By:
- Publication type:
- Letter
RARE DISEASE IN SOUTH-EASTERN EUROPE, 15-17 NOVEMBER 2012, SKOPJE, REPUBLIC OF MACEDONIA.
- Published in:
- 2012
- By:
- Publication type:
- Proceeding
CHILDREN BORN SMALL FOR GESTATIONAL AGE (SGA).
- Published in:
- Contributions of Macedonian Academy of Sciences & Arts, 2012, v. 33, n. 2, p. 47
- By:
- Publication type:
- Article
A GIANT OSTEOCHONDROMA IN A BOY WITH MULTIPLE EXOSTOSES.
- Published in:
- Contributions of Macedonian Academy of Sciences & Arts, 2011, v. 32, n. 2, p. 317
- By:
- Publication type:
- Article
ACUTE GALLBLADDER HYDROPS AND ARTHRITIS: UNUSUAL INITIAL MANIFESTATIONS OF WILSON'S DISEASE (WD).
- Published in:
- Contributions of Macedonian Academy of Sciences & Arts, 2011, v. 32, n. 2, p. 307
- By:
- Publication type:
- Article
HUNTER SYNDROME (MUCCOPOLYSACCHARRIDOSIS TYPE II) IN MACEDONIA AND BULGARIA.
- Published in:
- Contributions of Macedonian Academy of Sciences & Arts, 2011, v. 32, n. 2, p. 187
- By:
- Publication type:
- Article
EARLY-ONSET OCULAR OCHRONOSIS IN A GIRL WITH ALKAPTONURIA (AKU) AND A NOVEL MUTATION IN HOMOGENTISATE 1,2-DIOXYGENASE (HGD).
- Published in:
- 2011
- By:
- Publication type:
- Case Study
RARE DISEASES WITH RENAL INVOLVEMENT IN THE REPUBLIC OF MACEDONIA.
- Published in:
- Contributions of Macedonian Academy of Sciences & Arts, 2011, v. 32, n. 1, p. 55
- By:
- Publication type:
- Article
ON RARE AND "SUPER-RARE" DISEASES: AN INSIGHT FROM THE REPUBLIC OF MACEDONIA.
- Published in:
- Contributions of Macedonian Academy of Sciences & Arts, 2011, v. 32, n. 1, p. 7
- By:
- Publication type:
- Article
FOUR GENERATIONS IN A FAMILY WITH NEUROFIBROMATOSIS 1: PRECOCIOUS PUBERTY AND OPTIC NERVE TUMOR (OPT).
- Published in:
- 2010
- By:
- Publication type:
- Case Study
GROWTH HORMONE DEFICIENCY (GHD) AND SMALL FOR GESTATIONAL AGE (SGA): GENETIC ALTERATIONS.
- Published in:
- Contributions of Macedonian Academy of Sciences & Arts, 2009, v. 30, n. 2, p. 33
- By:
- Publication type:
- Article
TYPE I GAUCHER DISEASE (GDI) IN THREE SIBLINGS: ENZYME REPLACEMENT TREATMENT (ERT) REQUIRED.
- Published in:
- Contributions of Macedonian Academy of Sciences & Arts, 2009, v. 30, n. 1, p. 233
- By:
- Publication type:
- Article
Seroreactivity to Dirofilaria antigens in people from different areas of Serbia.
- Published in:
- BMC Infectious Diseases, 2014, v. 14, n. 1, p. 1, doi. 10.1186/1471-2334-14-68
- By:
- Publication type:
- Article