Nenad Blau
Blau, Nenad, 1946-....
Blau, N. (Nenad), 1946-
Blau, Nenad
Blau, N. 1946-
Blau, N. (Nenad)
VIAF ID: 112959702 (Personal)
Permalink: http://viaf.org/viaf/112959702
Preferred Forms
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- 100 1 _ ‡a Blau, N. ‡d 1946-
- 100 1 _ ‡a Blau, N. ‡q (Nenad)
- 100 1 _ ‡a Blau, N. ‡q (Nenad), ‡d 1946-
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- 100 1 _ ‡a Blau, Nenad ‡d 1946-
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- 100 1 _ ‡a Blau, Nenad, ‡d 1946-....
- 100 0 _ ‡a Nenad Blau
4xx's: Alternate Name Forms (13)
5xx's: Related Names (1)
Works
Title | Sources |
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1H-NMR studies with tetrahydrobiopterins, evidence for the structure of 6-pyruvoyltetrahydropterin, an intermediate in the biosynthesis of tetrahydrobiopterin | |
Aluminium and acid rain mitigating effects of NaCl on aluminium toxicity to brown trout (Salmo trutta Fario) in acid water | |
Chemistry and biology of pteridines 1989 pteridines and folic acid derivatives proceedings of the ninth International symposium on pteridines and folic acid derivatives, chemical, biological and clinical aspects, Zurich, Switzerland, September 3-8, 1989 | |
Congenital neurotransmitter disorders : a clinical approach | |
Homocistinurija : prikaz bolesnika uz osvrt na hiperhomocisteinemiju kao faktor rizika za ranu pojavu bolesti krvnih žila | |
hyperphenylalaninemias a differential diagnosis and international database of tetrahydrobiopterin deficiencies | |
Inherited disorders of biogenic amines: a practical guide | |
Laboratory guide to the methods in biochemical genetics | |
New approaches to treat PKU: how far are we? | |
Optimizing the use of sapropterin | |
Pathogenesis of cognitive dysfunction in phenylketonuria: review of hypotheses. | |
Phenylalanine hydroxylase-stimulating protein/pterin-4alpha-carbinolamine dehydratase from rat and human liver purification, characterization, and complete amino acid sequence | |
Phenylalanine loading as a diagnostic test for DRD: interpreting the utility of the test | |
Phenylketonuria and BH4 deficiencies | |
Physician's guide to the laboratory diagnosis of metabolic diseases | |
Possible impact of tetrahydrobiopterin and sepiapterin on endothelial dysfunction | |
Primapterinuria: a new variant of atypical phenylketonuria | |
Production of monoclonal antibodies against human 6-pyruvoyl tetrahydropterin synthase and immunocytochemical localization of the enzyme | |
Progress in the study of biosynthesis and role of 7-substituted pterins: function of pterin-4a-carbinolamine dehydratase | |
Psychomotor retardation, spastic paraplegia, cerebellar ataxia and dyskinesia associated with low 5-methyltetrahydrofolate in cerebrospinal fluid: a novel neurometabolic condition responding to folinic acid substitution | |
Pterins, folates and neurotransmitters in molecular medicine 13th international conference 2003, Maui/Hawaii | |
R208X mutation in CLN2 gene associated with reduced cerebrospinal fluid pterins in a girl with classic late infantile neuronal ceroid lipofuscinosis | |
Recessive mutations in PCBD1 cause a new type of early-onset diabetes | |
Reduced folate transport to the CNS in female Rett patients | |
Reduced nitric oxide metabolites in CSF of patients with tetrahydrobiopterin deficiency | |
Regulation of 6-pyruvoyltetrahydropterin synthase activity and messenger RNA abundance in human vascular endothelial cells | |
Retrovirus-mediated double transduction of the GTPCH and PTPS genes allows 6-pyruvoyltetrahydropterin synthase-deficient human fibroblasts to synthesize and release tetrahydrobiopterin. | |
Screening for tetrahydrobiopterin deficiency in newborns using dried urine on filter paper | |
Separation of low molecular weight proteins with SDS-PAGE using taurine as a new trailing ion. | |
Sepiapterin reductase deficiency: a treatable mimic of cerebral palsy. | |
Sepiapterin reductase deficiency an autosomal recessive DOPA-responsive dystonia. | |
Sepiapterin reductase deficiency in a 2-year-old girl with incomplete response to treatment during short-term follow-up. | |
Sepiapterin reductase deficiency: two Indian siblings with unusual clinical features | |
Serine 19 of human 6-pyruvoyltetrahydropterin synthase is phosphorylated by cGMP protein kinase II | |
Serum bile acids determined with an RA 1000 analyzer | |
Severe deformity of a Palmaz-Schatz stent after normal surgical manipulation. | |
Simple rapid method for the separation and quantitative analysis of carbohydrates in biological fluids | |
Simultaneous determination of oxalate, glycolate, citrate, and sulfate from dried urine filter paper spots in a pediatric population | |
The spectrum of phenylketonuria genotypes in the Armenian population: identification of three novel mutant PAH alleles | |
Splicing of phenylalanine hydroxylase (PAH) exon 11 is vulnerable: molecular pathology of mutations in PAH exon 11. | |
Spontaneous remission of Cushing's syndrome in a patient with an adrenal adenoma | |
Structural and Functional Consequences of Mutations in 6-Pyruvoyltetrahydropterin Synthase Causing Hyperphenylalaninemia in Humans | |
Suspected pterin-4a-carbinolamine dehydratase deficiency hyperphenylalaninaemia due to inhibition of phenylalanine hydroxylase by tetrahydro-7-biopterin | |
Systemic tetrahydrobiopterin (BH4) levels and coronary artery disease | |
Tetrahydrobiopterin in the Treatment of Infantile Hypertrophic Pyloric Stenosis | |
Tetrahydrobiopterin induced neonatal tyrosinaemia | |
Tetrahydrobiopterin is a secretory product of murine vascular endothelial cells. | |
Tetrahydrobiopterin, its mode of action on phenylalanine hydroxylase, and importance of genotypes for pharmacological therapy of phenylketonuria. | |
Tetrahydrobiopterin loading test in xanthine dehydrogenase and molybdenum cofactor deficiencies | |
Tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency: possible regulation of gene expression in a patient with the homozygous L48S mutation | |
Tetrahydrobiopterin responsiveness in phenylketonuria: prediction with the 48-hour loading test and genotype. | |
Tetrahydrobiopterin shows chaperone activity for tyrosine hydroxylase | |
Tetrahydrobiopterin synthesis precedes nitric oxide-dependent inhibition of insulin secretion in INS-1 rat pancreatic beta-cells. | |
There is no doubt that the early identification of PKU and prompt and continuous intervention prevents mental retardation in most patients. | |
Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis | |
Unconjugated pterins and related biogenic amines, 1987: | |
Unique aspects of sequence variant interpretation for inborn errors of metabolism (IEM): The ClinGen IEM Working Group and the Phenylalanine Hydroxylase Gene | |
Unusual Case of Phenylketonuria With Atypical Brain Magnetic Resonance Imaging Findings | |
Urinary saturation and nephrocalcinosis in preterm infants: effect of parenteral nutrition | |
Use of a ruthenium(III), iron(II), and nickel(II) hexacyanometallate-modified graphite electrode with immobilized oxalate oxidase for the determination of urinary oxalate | |
Value of the urinary stone promoters/inhibitors ratios in the estimation of the risk of urolithiasis |