BIOSYNTHESIS AND SECRETION OF CATALYTICALLY ACTIVE ACETYL CHOLINESTERASE IN XENOPUS OOCYTES MICROINJECTED WITH MRNA FROM RAT BRAIN AND FROM TORPEDO ELECTRIC ORGAN = BIOSYNTHESE ET SECRETION D'ACETYLCHOLINESTERASE CATALYTIQUEMENT ACTIVE DANS DES OOCYTES DE XENOPUS LAEVIS AYANT RECU PAR MICROINJECTION DE L'ARNM DE CERVEAU DE RAT ET D'ORGANE ELECTRIQUE DE TORPEDOSOREQ H; PARVARI R; SILMAN I et al.1982; PROC. NATL. ACAD. SCI. U.S.A., BIOL. SCI.; ISSN 0273-1134; USA; DA. 1982; VOL. 79; NO 3; PP. 830-834; BIBL. 53 REF.Article

INCREASE IN THE TRANSLATABLE MRNA FOR ACETYLCHOLINE RECEPTOR DURING EMBRYONIC DEVELOPMENT OF TORPEDO OCELLATA ELECTRIC ORGANSOREQ H; BARTFELD D; PARVARI R et al.1982; FEBS LETT.; ISSN 0014-5793; NLD; DA. 1982; VOL. 139; NO 1; PP. 32-36; BIBL. 21 REF.Article

A microfluorometric assay for cholinesterases, suitable for multiple kinetic determinations of picomoles of released thiocholinePARVARI, R; PECHT, I; SOREQ, H et al.Analytical biochemistry. 1983, Vol 133, Num 2, pp 450-456, issn 0003-2697Article

Transcription map of Xq27 : Candidates for several X-linked diseasesZUCCHI, I; JONES, J; MUMM, S et al.Genomics (San Diego, Calif.). 1999, Vol 57, Num 2, pp 209-218, issn 0888-7543Article

Glycogen storage disease type 1a in three siblings with the G270V mutationPARVARI, R; ISAM, J; MOSES, S. W et al.Journal of inherited metabolic disease. 1999, Vol 22, Num 2, pp 149-154, issn 0141-8955Article

Prenatal diagnosis of glycogen storage disease type 1a by single stranded conformation polymorphism (SSCP)PARVARI, R; HERSHKOVITZ, E; CARMI, R et al.Prenatal diagnosis. 1996, Vol 16, Num 9, pp 862-865, issn 0197-3851Article

Glycogen storage disease type 1a in Israel : Biochemical, clinical, and mutational studiesPARVARI, R; LEI, K.-J; BASHAN, N et al.American journal of medical genetics. 1997, Vol 72, Num 3, pp 286-290, issn 0148-7299Article

The 3849+10 kB C→T mutation in a 21-year-old patient with cystic fibrosisKAPLAR, D. M; NIV, A; AVIRAM, M et al.Ear, nose & throat journal. 1996, Vol 75, Num 12, pp 793-795, issn 0145-5613Article

Somatic diversification of chicken immunoglobulin light chains by point mutationsPARVARI, R; ZIV, E; LANTNER, F et al.Proceedings of the National Academy of Sciences of the United States of America. 1990, Vol 87, Num 8, pp 3072-3076, issn 0027-8424, 5 p.Article

Analyses of chicken immunoglobulin light chain cDNA clones indicate a few germline Vλ genes and allotypes of the Cλ locusPARVARI, R; ZIV, E; LENTNER, F et al.EMBO journal (Print). 1987, Vol 6, Num 1, pp 97-102, issn 0261-4189Article

Male hypogonadism due to a mutation in the gene for the β-subunit of follicle-stimulating hormonePHILLIP, M; ARBELLE, J. E; SEGEV, Y et al.The New England journal of medicine. 1998, Vol 338, Num 24, pp 1729-1732, issn 0028-4793Article

Two new mutations in the 3' coding region of the glycogen debranching enzyme in a glycogen storage disease type IIIa Ashkenazi Jewish patientPARVARI, R; SHEN, J; HERSHKOVITZ, E et al.Journal of inherited metabolic disease. 1998, Vol 21, Num 2, pp 141-148, issn 0141-8955Article

Ataxia with isolated Vitamin E deficiency in four siblingsSHORER, Z; PARVARI, R; BRIL, G et al.Pediatric neurology. 1996, Vol 15, Num 4, pp 340-343, issn 0887-8994Article

RFLPs for linkage analysis in families with glycogen storage disease type IIIMISHORI-DERY, A; BASHAN, N; MOSES, S et al.Journal of inherited metabolic disease. 1995, Vol 18, Num 2, pp 207-210, issn 0141-8955Article

Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42-43PARVARI, R; HERSHKOVITZ, E; KANIS, A et al.American journal of human genetics. 1998, Vol 63, Num 1, pp 163-169, issn 0002-9297Article

The gene for glycogen-storage disease type 1b maps to chromosome 11q23ANNABI, B; HIRAIWA, H; FRYMAN, M et al.American journal of human genetics. 1998, Vol 62, Num 2, pp 400-405, issn 0002-9297Article

Characterization of the mutations in the glucose-6-phosphatase gene in Israeli patients with glycogen storage disease type 1a: R83C in six Jews and a novel V166G mutation in a Muslim ArabPARVARI, R; MOSES, S; HERSHKOVITZ, E et al.Journal of inherited metabolic disease. 1995, Vol 18, Num 1, pp 21-27, issn 0141-8955Article

Chicken immunoglobulin γ-heavy chains: limited VH gene repertoire, combinatorial diversification by D gene segments and evolution of the heavy chain locusPARVARI, R; AVIVI, A; LENTNER, F et al.EMBO journal (Print). 1988, Vol 7, Num 3, pp 739-744, issn 0261-4189Article

Congenital insensitivity to pain: Orthopaedic manifestationsBAR-ON, E; WEIGL, D; PARVARI, R et al.Journal of bone and joint surgery. British volume. 2002, Vol 84, Num 2, pp 252-257, issn 0301-620XArticle

Short stature in carriers of recessive mutation causing familial isolated growth hormone deficiencyLEIBERMAN, E; PESLER, D; PARVARI, R et al.American journal of medical genetics. 2000, Vol 90, Num 3, pp 188-192, issn 0148-7299Article

Deletion of 8.5 Mb, including the FMR1 gene, in a male with the fragile X syndrome phenotype and overgrowthPARVARI, R; MUMM, S; GALIL, A et al.American journal of medical genetics. 1999, Vol 83, Num 4, pp 302-307, issn 0148-7299Article

Linkage localization of the thoraco-abdominal syndrome (TAS) gene to Xq25-26PARVARI, R; WEINSTEIN, Y; EHRLICH, S et al.American journal of medical genetics. 1994, Vol 49, Num 4, pp 431-434, issn 0148-7299Article