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351. Effectiveness of Planned Teaching Programme on Knowledge Regarding Prevention of Depression in Adolescents Among the Parents of Adolescents in Selected Secondary Schools of Mumbai City

352. Vitamin B-6 vitamers in human plasma and cerebrospinal fluid

353. Comment on Zwickler et al.: Usefulness of biochemical parameters in decision-making on the start of emergency treatment in patients with propionic acidemia

354. Irreversible brain creatine deficiency with elevated serum and urine creatine: A creatine transporter defect?

355. Phytanoyl-CoA hydroxylase activity is induced by phytanic acid

356. Mental retardation and behavioral problems as presenting signs of a creatine synthesis defect

357. Facial anomalies inD-2-hydroxyglutaric aciduria

358. A new approach for fast metabolic diagnostics in CMAMMA

359. Effectiveness of whole-exome sequencing and costs of the traditional diagnostic trajectory in children with intellectual disability

361. Development of psychopathology in deployed armed forces in relation to plasma GABA levels

362. The value of plasma vitamin B6 profiles in early onset epileptic encephalopathies

363. A new approach for fast metabolic diagnostics in CMAMMA

364. Effectiveness of whole-exome sequencing and costs of the traditional diagnostic trajectory in children with intellectual disability

365. Development of psychopathology in deployed armed forces in relation to plasma GABA levels

366. CSF d-serine concentrations are similar in Alzheimer's disease, other dementias, and elderly controls

367. The value of plasma vitamin B6 profiles in early onset epileptic encephalopathies

370. Effectiveness of whole-exome sequencing and costs of the traditional diagnostic trajectory in children with intellectual disability

371. The value of plasma vitamin B6 profiles in early onset epileptic encephalopathies

373. Sandwich-Architectured Poly(lactic acid)–Graphene Composite Food Packaging Films

374. ASSOCIATION BETWEEN VITAMIN B6 AND WHITE MATTER HYPERINTENSITIES IN PATIENTS WITH ALZHEIMER'S DISEASE NOT MEDIATED BY HOMOCYSTEINE METABOLISM

375. Iron Release From Human Monocytes After Erythrophagocytosis In Vitro: An Investigation in Normal Subjects and Hereditary Hemochromatosis Patients

376. Phytanic acid and pristanic acid are oxidized by sequential peroxisomal and mitochondrial reactions in cultured fibroblasts

377. Overexpression of GAMT restores GAMT activity in primary GAMT-deficient fibroblasts

378. Monocarboxylate transporter 1 deficiency and ketone utilization

379. Phytanic acid α-oxidation in peroxisomal disorders: Studies in cultured human fibroblasts

380. The transmethylation cycle in the brain of Alzheimer patients

381. The potential of exosomes in diagnosis and treatment of inborn errors of metabolism

382. Atypical Vitamin B-6 Deficiency A Rare Cause of Unexplained Neonatal and Infantile Epilepsies

383. D-amino acid aberrations in cerebrospinal fluid and plasma of smokers

384. An update on serine deficiency disorders

386. Supplementation with a powdered blend of PUFAs normalizes DHA and AA levels in patients with PKU

387. Reliable analysis of phenylalanine and tyrosine in a minimal volume of blood

389. Design of Electronic Nose System Using Gas Chromatography Principle and Surface Acoustic Wave Sensor.

390. Interplay between metabolic identities in the intestinal crypt supports stem cell function

391. Enzyme Assay for Diagnosis of Guanidinoacetate Methyltransferase Deficiency

392. Mutations in the AGXT2L2 gene cause phosphohydroxylysinuria

393. The malate-aspartate shuttle is important for de novo serine biosynthesis.

394. Diagnostic Enzyme Assay That Uses Stable-Isotope-labeled Substrates to Detect l-Arginine:Glycine Amidinotransferase Deficiency

395. The intestine plays a substantial role in human vitamin B6 metabolism: a Caco-2 cell model

396. A Common Variant in ERBB4 Regulates GABA Concentrations in Human Cerebrospinal Fluid

397. Vitamin B6 vitamer concentrations in cerebrospinal fluid differ between preterm and term newborn infants

398. Identification of a Human trans-3-Hydroxy-L-proline Dehydratase, the First Characterized Member of a Novel Family of Proline Racemase-like Enzymes

399. Structural analysis of the Leptospiral sphingomyelinases: in silico and experimental evaluation of Sph2 as an Mg-dependent sphingomyelinase

400. Impaired cognitive functioning in patients with tyrosinemia type I receiving nitisinone

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