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Ali Naini

Research Profile

Chemicals & Drugs

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Publications

TOP 3
Sara Shanske; Hasan O Akman; Ramen Chmait; Michio Hirano; Jiesheng Lu; Mahesh Mansukhani; Ali Naini; Salvatore DiMauro
Mutation in an mtDNA protein-coding gene: prenatal diagnosis aided by fetal muscle biopsy.
Chunmei Qiu; James J Russo; Eric A Schon; Shundi Shi; Sergey M Kalachikov; Shiv Kumar; Jiesheng Lu; Ali Naini; J Guo; Jingyue Ju
Mitochondrial single nucleotide polymorphism genotyping by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry using cleavable biotinylated dideoxynucleotides.
Valentina Emmanuele; Andres Berardo; Erin D'Agostino; Salvatore DiMauro; Luis C López; Ali Naini; Catarina Quinzii; Martha Solomon; Saba Tadesse; Bing Wen; Luis López; Michio Hirano
Heterogeneity of coenzyme Q10 deficiency: patient study and literature review.

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All Publications

2013: Sara Shanske; Hasan O Akman; Ramen Chmait; Michio Hirano; Jiesheng Lu; Mahesh Mansukhani; Ali Naini; Salvatore DiMauro
Mutation in an mtDNA protein-coding gene: prenatal diagnosis aided by fetal muscle biopsy.
Journal of child neurology 2013;28(2):264-8.
2012: Chunmei Qiu; James J Russo; Eric A Schon; Shundi Shi; Sergey M Kalachikov; Shiv Kumar; Jiesheng Lu; Ali Naini; J Guo; Jingyue Ju
Mitochondrial single nucleotide polymorphism genotyping by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry using cleavable biotinylated dideoxynucleotides.
Analytical biochemistry 2012;427(2):202-10.
2012: Valentina Emmanuele; Andres Berardo; Erin D'Agostino; Salvatore DiMauro; Luis C López; Ali Naini; Catarina Quinzii; Martha Solomon; Saba Tadesse; Bing Wen; Luis López; Michio Hirano
Heterogeneity of coenzyme Q10 deficiency: patient study and literature review.
Archives of neurology 2012;69(8):978-83.
2012: Catarina M Quinzii; Saba Tadesse; Ali Naini; Michio Hirano
Effects of inhibiting CoQ10 biosynthesis with 4-nitrobenzoate in human fibroblasts.
PloS one 2012;7(2):e30606.
2010: Salvatore DiMauro; Caterina Garone; Ali Naini
Metabolic myopathies.
Current rheumatology reports 2010;12(5):386-93.
2010: Catarina M Quinzii; Luis Lopez; Robert W Gilkerson; Beatriz Dorado; Jorida Coku; Ali Naini; Clotilde Lagier-Tourenne; Markus Schuelke; Leonardo Salviati; Rosalba Carrozzo; Filippo Santorelli; Shamima Rahman; Meriem Tazir; Michel Koenig; Salvatore DiMauro; Michio Hirano
Reactive oxygen species, oxidative stress, and cell death correlate with level of CoQ10 deficiency.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2010;24(10):3733-43.
2010: Jorida Coku; Sara Shanske; Mahsa Mehrazin; Kurenai Tanji; Ali Naini; Valentina Emmanuele; Marc Patterson; Michio Hirano; Salvatore DiMauro
Slowly progressive encephalopathy with hearing loss due to a mutation in the mtDNA tRNA(Leu(CUN)) gene.
Journal of the neurological sciences 2010;290(1-2):166-8.
2010: Bulent Kurt; Jaak Jaeken; Johan Van Hove; Lieven Lagae; Ann Löfgren; David B Everman; Parul Jayakar; Ali Naini; Klaas Jan Wierenga; Gert Van Goethem; William C Copeland; Salvatore DiMauro
A novel POLG gene mutation in 4 children with Alpers-like hepatocerebral syndromes.
Archives of neurology 2010;67(2):239-44.
2010: Luis C López; Catarina M Quinzii; Estela Area; Ali Naini; Shamima Rahman; Markus Schuelke; Leonardo Salviati; Salvatore DiMauro; Michio Hirano
Treatment of CoQ(10) deficient fibroblasts with ubiquinone, CoQ analogs, and vitamin C: time- and compound-dependent effects.
PloS one 2010;5(7):e11897.
2009: Ali Naini; Antonio Toscano; Olimpia Musumeci; John Vissing; Hasan O Akman; Salvatore DiMauro
Muscle phosphoglycerate mutase deficiency revisited.
Archives of neurology 2009;66(3):394-8.
2009: Mahsa Mehrazin; Sara Shanske; Petra Kaufmann; Ying Wei; Jorida Coku; Kristin Engelstad; Ali Naini; Darryl C De Vivo; Salvatore DiMauro
Longitudinal changes of mtDNA A3243G mutation load and level of functioning in MELAS.
American journal of medical genetics. Part A 2009;149A(4):584-7.
2008: Kurenai Tanji; Petra Kaufmann; Ali Naini; Jiesheng Lu; Timothy C Parsons; Dong Wang; Joshua Z Willey; Sara Shanske; Michio Hirano; Eduardo Bonilla; Alexander Khandji; Salvatore DiMauro; Lewis P Rowland
A novel tRNA(Val) mitochondrial DNA mutation causing MELAS.
Journal of the neurological sciences 2008;270(1-2):23-7.
2008: Catarina M Quinzii; Luis Lopez; Jakob Von-Moltke; Ali Naini; Sindu Krishna; Markus Schuelke; Leonardo Salviati; Plácido Navas; Salvatore DiMauro; Michio Hirano
Respiratory chain dysfunction and oxidative stress correlate with severity of primary CoQ10 deficiency.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2008;22(6):1874-85.
2008: Michio Hirano; Corrado Angelini; Pasquale Montagna; Arthur P Hays; Kurenai Tanji; Hiroshi Mitsumoto; Paul H Gordon; Ali Naini; Salvatore DiMauro; Lewis P Rowland
Amyotrophic lateral sclerosis with ragged-red fibers.
Archives of neurology 2008;65(3):403-6.
2008: Sara Shanske; Jorida Coku; Jiesheng Lu; Jai Ganesh; Sindu Krishna; Kurenai Tanji; Eduardo Bonilla; Ali Naini; Michio Hirano; Salvatore DiMauro
The G13513A mutation in the ND5 gene of mitochondrial DNA as a common cause of MELAS or Leigh syndrome: evidence from 12 cases.
Archives of neurology 2008;65(3):368-72.
2007: Klaus Gempel; Haluk Topaloglu; Beril Talim; Peter Schneiderat; Benedikt Schoser; Volkmar H Hans; Beatrix Pálmafy; Gülsev Kale; Aysegul Tokatli; Catarina M Quinzii; Michio Hirano; Ali Naini; Salvatore DiMauro; Holger Prokisch; Hanns Lochmüller; Rita Horvath
The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene.
Brain : a journal of neurology 2007;130(Pt 8):2037-44.
2007: Ali Naini; Mahsa Mehrazin; Jiesheng Lu; Paul Gordon; Hiroshi Mitsumoto
Identification of a novel D109Y mutation in Cu/Zn superoxide dismutase (sod1) gene associated with amyotrophic lateral sclerosis.
Journal of the neurological sciences 2007;254(1-2):17-21.
2007: Ali Naini; Sara Shanske
Detection of mutations in mtDNA.
Methods in cell biology 2007;80():437-63.
2006: Luis Lopez; Markus Schuelke; Catarina M Quinzii; Tomotake Kanki; Richard J T Rodenburg; Ali Naini; Salvatore DiMauro; Michio Hirano
Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutations.
American journal of human genetics 2006;79(6):1125-9.
2006: Shin J Oh; Kyung-Seok Park; Hewitt F Ryan; Moris J Danon; Jiesheng Lu; Ali Naini; Salvatore DiMauro
Exercise-induced cramp, myoglobinuria, and tubular aggregates in phosphoglycerate mutase deficiency.
Muscle & nerve 2006;34(5):572-6.
2006: Arthur P Hays; Ali Naini; Cui Zhen He; Hiroshi Mitsumoto; Lewis P Rowland
Sporadic amyotrophic lateral sclerosis and breast cancer: Hyaline conglomerate inclusions lead to identification of SOD1 mutation.
Journal of the neurological sciences 2006;242(1-2):67-9.
2006: R K Shepherd; Nicoletta Checcarelli; Ali Naini; Darryl C De Vivo; Salvatore DiMauro; Carolyn M Sue
Measurement of ATP production in mitochondrial disorders.
Journal of inherited metabolic disease 2006;29(1):86-91.
2006: Catarina M Quinzii; Ali Naini; Leonardo Salviati; Eva Trevisson; Plácido Navas; Salvatore DiMauro; Michio Hirano
A mutation in para-hydroxybenzoate-polyprenyl transferase (COQ2) causes primary coenzyme Q10 deficiency.
American journal of human genetics 2006;78(2):345-9.
2006: Rita Horvath; Peter Schneiderat; Benedikt Schoser; Klaus Gempel; E Neuen-Jacob; H Plöger; Josef Müller-Höcker; Dieter Pongratz; Ali Naini; Salvatore DiMauro; Hanns Lochmüller
Coenzyme Q10 deficiency and isolated myopathy.
Neurology 2006;66(2):253-5.
2006: Heiner K. Berthold; Ali Naini; Salvatore Di Mauro; Merja Hallikainen; Helena Gylling; Wilhelm Krone; Ioanna Gouni-Berthold
Effect of ezetimibe and/or simvastatin on coenzyme Q10 levels in plasma: a randomised trial.
Drug safety : an international journal of medical toxicology and drug experience 2006;29(8):703-12.
2005: Costanza Lamperti; Ali Naini; Valeria Lucchini; Alessandro Prelle; Nereo Bresolin; Maurizio Moggio; Monica Sciacco; Petra Kaufmann; Salvatore DiMauro
Muscle coenzyme Q10 level in statin-related myopathy.
Archives of neurology 2005;62(11):1709-12.
2005: Leonardo Salviati; Sabrina Sacconi; Luisa Murer; Graziella Zacchello; L Franceschini; Anna Maria Laverda; Giuseppe Basso; Catarina M Quinzii; Corrado Angelini; Michio Hirano; Ali Naini; Plácido Navas; Salvatore DiMauro; Giovanni Montini
Infantile encephalomyopathy and nephropathy with CoQ10 deficiency: a CoQ10-responsive condition.
Neurology 2005;65(4):606-8.
2005: Ali Naini; Petra Kaufmann; Sara Shanske; Kristin Engelstad; Darryl C De Vivo; Eric A Schon
Hypocitrullinemia in patients with MELAS: an insight into the "MELAS paradox".
Journal of the neurological sciences 2005;229-230():187-93.
2005: Ali Naini; Jiesheng Lu; Petra Kaufmann; Richard A Bernstein; Michelangelo Mancuso; Eduardo Bonilla; Michio Hirano; Salvatore DiMauro
Novel mitochondrial DNA ND5 mutation in a patient with clinical features of MELAS and MERRF.
Archives of neurology 2005;62(3):473-6.
2005: Catarina M Quinzii; A G Kattah; Ali Naini; Hasan O Akman; V K Mootha; Salvatore DiMauro; Michio Hirano
Coenzyme Q deficiency and cerebellar ataxia associated with an aprataxin mutation.
Neurology 2005;64(3):539-41.
2004: Sara Shanske; Jacklyn Pancrudo; Petra Kaufmann; Kristin Engelstad; Sarah Jhung; Jiesheng Lu; Ali Naini; Salvatore DiMauro; Darryl C De Vivo
Varying loads of the mitochondrial DNA A3243G mutation in different tissues: implications for diagnosis.
American journal of medical genetics. Part A 2004;130A(2):134-7.
2004: Conrad L Leung; Cui Zhen He; Petra Kaufmann; Steven S Chin; Ali Naini; Ronald K H Liem; Hiroshi Mitsumoto; Arthur P Hays
A pathogenic peripherin gene mutation in a patient with amyotrophic lateral sclerosis.
Brain pathology (Zurich, Switzerland) 2004;14(3):290-6.
2004: Tatjana Rundek; Ali Naini; Ralph L Sacco; Kristen Coates; Salvatore DiMauro
Atorvastatin decreases the coenzyme Q10 level in the blood of patients at risk for cardiovascular disease and stroke.
Archives of neurology 2004;61(6):889-92.
2004: Salvatore DiMauro; Michelangelo Mancuso; Ali Naini
Mitochondrial encephalomyopathies: therapeutic approach.
Annals of the New York Academy of Sciences 2004;1011():232-45.
2004: Maira Gironi; Costanza Lamperti; Raffaello Nemni; Maurizio Moggio; Giancarlo Comi; Franca R Guerini; Pasquale Ferrante; Nicola Canal; Ali Naini; Nereo Bresolin; Salvatore DiMauro
Late-onset cerebellar ataxia with hypogonadism and muscle coenzyme Q10 deficiency.
Neurology 2004;62(5):818-20.
2003: Kim Tieu; Celine Perier; Casper Caspersen; Peter Teismann; Du-Chu Wu; Shi Du Yan; Ali Naini; Miquel Vila; Vernice Jackson-Lewis; Ravichandran Ramasamy; Serge Przedborski
D-beta-hydroxybutyrate rescues mitochondrial respiration and mitigates features of Parkinson disease.
The Journal of clinical investigation 2003;112(6):892-901.
2003: Merlin G Butler; Majed Dasouki; Douglas C Bittel; Susan Hunter; Ali Naini; Salvatore DiMauro
Coenzyme Q10 levels in Prader-Willi syndrome: comparison with obese and non-obese subjects.
American journal of medical genetics. Part A 2003;119A(2):168-71.
2003: Peter Teismann; Kim Tieu; Dong-Kug Choi; Du-Chu Wu; Ali Naini; Stéphane Hunot; Miquel Vila; Vernice Jackson-Lewis; Serge Przedborski
Cyclooxygenase-2 is instrumental in Parkinson's disease neurodegeneration.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(9):5473-8.
2003: Costanza Lamperti; Ali Naini; Michio Hirano; Darryl C De Vivo; E Bertini; Serenella Servidei; M Valeriani; D Lynch; B Banwell; M Berg; T Dubrovsky; Claudia A Chiriboga; Corrado Angelini; Elena Pegoraro; Salvatore DiMauro
Cerebellar ataxia and coenzyme Q10 deficiency.
Neurology 2003;60(7):1206-8.
2003: Maya R Vilà; Toni Segovia-Silvestre; Josep Gámez; Alberto Marina; Ali Naini; Anna Meseguer; A Lombès; Eduardo Bonilla; Salvatore DiMauro; Michio Hirano; Antoni L Andreu
Reversion of mtDNA depletion in a patient with TK2 deficiency.
Neurology 2003;60(7):1203-5.
2003: Sabrina Sacconi; Leonardo Salviati; Carolyn M Sue; Sara Shanske; Mercy M Davidson; Eduardo Bonilla; Ali Naini; Darryl C De Vivo; Salvatore DiMauro
Mutation screening in patients with isolated cytochrome c oxidase deficiency.
Pediatric research 2003;53(2):224-30.
2003: Ali Naini; Vernice-Jackson Lewis; Michio Hirano; Salvatore DiMauro
Primary coenzyme Q10 deficiency and the brain.
BioFactors (Oxford, England) 2003;18(1-4):145-52.
2002: Michelangelo Mancuso; Massimiliano Filosto; Ali Naini; Anna Rocchi; Alberto Del Corona; Ferdinando Sartucci; Gabriele Siciliano; Luigi Murri
A screening for superoxide dismutase-1 D90A mutation in Italian patients with sporadic amyotrophic lateral sclerosis.
Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases 2002;3(4):215-8.
2002: Ramon Marti; antonella spinazzola; Ichizo Nishino; Antoni L Andreu; Ali Naini; Saba Tadesse; Juan A Oliver; Michio Hirano
Mitochondrial neurogastrointestinal encephalomyopathy and thymidine metabolism: results and hypotheses.
Mitochondrion 2002;2(1-2):143-7.
2002: Georgios M Hadjigeorgiou; Menachem Sadeh; Olimpia Musumeci; Ron Dabby; Laura De Girolami; Ali Naini; Alexandros Papadimitriou; Sara Shanske; Salvatore DiMauro
Molecular genetic study of myophosphorylase deficiency (McArdle's disease) in two Yemenite-Jewish families.
Neuromuscular disorders : NMD 2002;12(9):824-7.
2002: Michelangelo Mancuso; Leonardo Salviati; Sabrina Sacconi; David Otaegui; Pilar Camaño; Alberto Marina; Sandra R Bacman; Carlos T Moraes; Jose R Carlo; M Garcia; M Garcia-Alvarez; L Monzon; Ali Naini; Michio Hirano; Eduardo Bonilla; A L Taratuto; Salvatore DiMauro; Tuan H Vu
Mitochondrial DNA depletion: mutations in thymidine kinase gene with myopathy and SMA.
Neurology 2002;59(8):1197-202.
2002: Leonardo Salviati; Sabrina Sacconi; Michelangelo Mancuso; David Otaegui; Pilar Camaño; Alberto Marina; Simon Rabinowitz; Rebecca Shiffman; Karen Thompson; Claire M Wilson; Annette Feigenbaum; Ali Naini; Michio Hirano; Eduardo Bonilla; Salvatore DiMauro; Tuan H Vu
Mitochondrial DNA depletion and dGK gene mutations.
Annals of neurology 2002;52(3):311-7.
2002: Ali Naini; Olimpia Musumeci; L Hayes; Francesco Pallotti; Maura L Del Bene; Hiroshi Mitsumoto
Identification of a novel mutation in Cu/Zn superoxide dismutase gene associated with familial amyotrophic lateral sclerosis.
Journal of the neurological sciences 2002;198(1-2):17-9.
2002: antonella spinazzola; Ramon Marti; Ichizo Nishino; Antoni L Andreu; Ali Naini; Saba Tadesse; Ivana Pela; Enrico Zammarchi; Maria Alice Donati; Juan A Oliver; Michio Hirano
Altered thymidine metabolism due to defects of thymidine phosphorylase.
The Journal of biological chemistry 2002;277(6):4128-33.
2002: Eric A Schon; Ali Naini; Sara Shanske
Identification of mutations in mtDNA from patients suffering mitochondrial diseases.
Methods in molecular biology (Clifton, N.J.) 2002;197():55-74.
2002: Serge Przedborski; Vernice Jackson-Lewis; David Sulzer; Ali Naini; Norma Romero; Caiping Chen; Julia Arias
Transgenic superoxide dismutase overproducer: murine.
Methods in enzymology 2002;349():180-90.
2001: Olimpia Musumeci; Ali Naini; A E Slonim; N Skavin; G L Hadjigeorgiou; N Krawiecki; B M Weissman; Chang-Yong Tsao; Jerry R Mendell; Sara Shanske; Darryl C De Vivo; Michio Hirano; Salvatore DiMauro
Familial cerebellar ataxia with muscle coenzyme Q10 deficiency.
Neurology 2001;56(7):849-55.
2001: Serge Przedborski; Vernice Jackson-Lewis; Ali Naini; Michael W Jakowec; Giselle M Petzinger; R Miller; M Akram
The parkinsonian toxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP): a technical review of its utility and safety.
Journal of neurochemistry 2001;76(5):1265-74.
2001: Gabriele Almer; Christelle Guégan; Peter Teismann; Ali Naini; Gorazd Rosoklija; Arthur P Hays; C Chen; Serge Przedborski
Increased expression of the pro-inflammatory enzyme cyclooxygenase-2 in amyotrophic lateral sclerosis.
Annals of neurology 2001;49(2):176-85.
2001: Giovanni Manfredi; antonella spinazzola; Nicoletta Checcarelli; Ali Naini
Assay of mitochondrial ATP synthesis in animal cells.
Methods in cell biology 2001;65():133-45.
1998: David W Desmond; Joan T Moroney; T Lynch; Stephen Chan; Steven S Chin; Dikoma Shungu; Ali Naini; Jay P Mohr
CADASIL in a North American family: clinical, pathologic, and radiologic findings.
Neurology 1998;51(3):844-9.
1998: J Ara; Serge Przedborski; Ali Naini; Vernice Jackson-Lewis; R R Trifiletti; J Horwitz; H Ischiropoulos
Inactivation of tyrosine hydroxylase by nitration following exposure to peroxynitrite and 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP).
Proceedings of the National Academy of Sciences of the United States of America 1998;95(13):7659-63.
1996: Serge Przedborski; D M Donaldson; Peregrine L Murphy; O Hirsch; D Lange; Ali Naini; D McKenna-Yasek; R H Brown
Blood superoxide dismutase, catalase and glutathione peroxidase activities in familial and sporadic amyotrophic lateral sclerosis.
Neurodegeneration : a journal for neurodegenerative disorders, neuroprotection, and neuroregeneration 1996;5(1):57-64.
1996: Tinmarla Frances Oo; Ali Naini; Robert E Burke
Augmented pharmacologic stimulation of striatal acetylcholine release following developmental hypoxic-ischemic injury.
Brain research 1996;706(1):145-50.
1996: C Raftopoulos; S Dethy; Marie-Aline Laute; Serge Goldman; Ali Naini; Serge Przedborski; J Hildebrand
Slow increase of homovanillic acid in cerebrospinal fluid after levodopa administration.
Movement disorders : official journal of the Movement Disorder Society 1996;11(1):59-62.
1995: Serge Przedborski; Marc Levivier; C Raftopoulos; Ali Naini; J Hildebrand
Peripheral and central pharmacokinetics of apomorphine and its effect on dopamine metabolism in humans.
Movement disorders : official journal of the Movement Disorder Society 1995;10(1):28-36.
1994: TG Nygaard; S P Waran; R A Levine; Ali Naini; A M Chutorian
Dopa-responsive dystonia simulating cerebral palsy.
Pediatric neurology 1994;11(3):236-40.
1993: Serge Przedborski; Vernice Jackson-Lewis; U Muthane; H Jiang; M Ferreira; Ali Naini; Stanley Fahn
Chronic levodopa administration alters cerebral mitochondrial respiratory chain activity.
Annals of neurology 1993;34(5):715-23.
1993: Ali Naini; E Vontzalidou; Lucien J Cote
Isocratic HPLC assay with electrochemical detection of free gamma-aminobutyric acid in cerebrospinal fluid.
Clinical chemistry 1993;39(2):247-50.
1992: Daniel H Fine; C Mendieta; M L Barnett; David Furgang; Ali Naini; J W Vincent
Endotoxin levels in periodontally healthy and diseased sites: correlation with levels of gram-negative bacteria.
Journal of periodontology 1992;63(11):897-901.
1992: Mary Sano; Karen Bell; Lucien J Cote; G Dooneief; A Lawton; L Legler; Karen Marder; Ali Naini; Yaakov Stern; Richard Mayeux
Double-blind parallel design pilot study of acetyl levocarnitine in patients with Alzheimer's disease.
Archives of neurology 1992;49(11):1137-41.
1992: Serge Przedborski; V Kostic; Vernice Jackson-Lewis; Ali Naini; S Simonetti; Stanley Fahn; E Carlson; C J Epstein; J L Cadet
Transgenic mice with increased Cu/Zn-superoxide dismutase activity are resistant to N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced neurotoxicity.
The Journal of neuroscience : the official journal of the Society for Neuroscience 1992;12(5):1658-67.
1991: E Fazzini; andrew dwork; C Blum; R Burke; Lucien J Cote; Robert R Goodman; T P Jacobs; Ali Naini; G Pezzoli; Seth L Pullman
Stereotaxic implantation of autologous adrenal medulla into caudate nucleus in four patients with parkinsonism. One-year follow-up.
Archives of neurology 1991;48(8):813-20.
1990: F Arnal; L J Coté; S Ginsburg; G D Lawrence; Ali Naini; Mary Sano
Studies on new, centrally active and reversible acetylcholinesterase inhibitors.
Neurochemical research 1990;15(6):587-91.
1989: Ali Naini; B Morgan; I D Mandel
Effect of protein malnutrition on the composition of submandibular glands of aged rats.
Archives of oral biology 1989;34(12):985-8.