A. Hays

H. Mitsumoto, L. Rowland, A. Hays, 2011, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Lymphoproliferative disorders and motor neuron disease

E D Louis, R. Lovelace, E. Louis, 1997, Neurology.

Gangliosides GM1 and GD1b are antigens for IgM M-protein in a patient with motor neuron disease

A. Hays, N. Latov, R. Yu, 1986, Neurology.

Monoclonal IgM with unique specificity to gangliosides GM1 and GD1b and to lacto‐N ‐tetraose associated with human motor neuron disease

E. Kabat, J. Albers, M. Shy, 1988, Neurology.

Lymphoma, motor neuron diseases, and amyotrophic lateral sclerosis

R. Lovelace, G. Inghirami, L. Rowland, 1991, Annals of neurology.

Neurolymphomatosis

R. Lovelace, G. Inghirami, R. Diaz-Arrastia, 1992, Neurology.

Amyotrophic lateral sclerosis and lymphoma

L. Rowland, A. Hays, N. Latov, 1992, Neurology.

Peripherin and Neurofilament Protein Coexist in Spinal Spheroids of Motor Neuron Disease

A. Hays, M. Corbo, 1992, Journal of neuropathology and experimental neurology.

Disorders of carbohydrate metabolism.

S. Dimauro, A. Hays, O. Akman, 2007, Handbook of clinical neurology.

HEPATIC LIPID METABOLISM IN THE CORTISONE-TREATED RAT.

A. Hays, R. Hill, W. E. Droke, 1965, Experimental and molecular pathology.

Autoantigens in human neuroblastoma cells

R. Liem, M. Mena, A. Hays, 1990, Journal of Neuroimmunology.

Axonal neuropathy in a patient with IgM M‐protein reactive with nerve endoneuriurn

A. Hays, N. Latov, L. Freddo, 1985, Neurology.

A novel mutation in PNPLA2 leading to neutral lipid storage disease with myopathy.

S. Dimauro, A. Hays, M. Hirano, 2012, Archives of neurology.

The neuromuscular manifestations of human immunodeficiency virus infections.

A. Hays, C. Britton, D. Lange, 1988, Archives of neurology.

Familial amyloidotic polyneuropathy presenting with carpal tunnel syndrome and a new transthyretin mutation, asparagine 70

A. Hays, R. Martone, D. Younger, 1992, Neurology.

Progressive multifocal leukoencephalopathy in a male homosexual with T-cell immune deficiency.

A. Hays, M. Tapper, C. Britton, 1982, The New England journal of medicine.

Axonal degeneration accompanied by conduction block induced by toxin mediated immune reactivity to GM1 ganglioside in rat nerves

G. Rosoklija, W. Trojaborg, A. Hays, 1995, Journal of the Neurological Sciences.

Localization of GM1 and Gal(β1‐3)GalNAc antigenic determinants in peripheral nerve

A. Hays, A. Quattrini, M. Corbo, 1993, Neurology.

Experimental conduction block induced by serum from a patient with anti‐GM1 antibodies

S. Staugaitis, A. Hays, M. Corbo, 1992, Annals of neurology.

A fatal case of coxsackievirus B4 meningoencephalitis.

Bruce Cree, A. Hays, G. Lowe, 2003, Archives of neurology.

Intravascular malignant lymphomatosis with neurological symptoms

R. Nemni, A. Hays, M. Corbo, 1996, Journal of Neurology.

Granulomatous angiitis of the nervous system.

A. Hays, L. Calabrese, D. Younger, 1997, Neurologic clinics.

A Pathogenic Peripherin Gene Mutation in a Patient with Amyotrophic Lateral Sclerosis

S. Chin, H. Mitsumoto, R. Liem, 2004, Brain pathology.

Anti‐MAG and anti‐SGPG antibodies in neuropathy

G. Rosoklija, L. H. van den Berg, R. Lovelace, 1996, Muscle & nerve.

Experimental autoimmune neuropathy with anti-GM1 antibodies and immunoglobulin deposits at the nodes of Ranvier

W. Trojaborg, A. Hays, N. Latov, 2004, Acta Neuropathologica.

Patterns of reactivity of human anti‐GM1 antibodies with spinal cord and motor neurons

A. Lugaresi, A. Hays, A. Quattrini, 1992, Annals of neurology.

Multifocal motor neuropathy with conduction block

R. Lovelace, W. Trojaborg, L. Rowland, 1992, Neurology.

Identification of glycoconjugates which are targets for anti-Gal(β1-3)GalNAc autoantibodies in spinal motor neurons

A. Lugaresi, A. Hays, M. Corbo, 1991, Journal of Neuroimmunology.

IgM deposits at nodes of ranvier in a patient with amyotrophic lateral sclerosis, anti‐GM1 antibodies, and multifocal motor conduction block

A. Hays, N. Latov, A. Uncini, 1990, Annals of neurology.

The spectrum of neurologic disease associated with anti‐GM1 antibodies

L. Berg, R. Lovelace, T. Munsat, 1990, Neurology.

Localization of neural epitopes that bind to IgM monoclonal autoantibodies (M-proteins) from two patients with motor neuron disease

A. Hays, N. Latov, F. P. Thomas, 1989, Journal of Neuroimmunology.

Small fiber neuropathy following vaccination for rabies, varicella or Lyme disease.

S. Ajroud‐Driss, A. Hays, H. Sander, 2009, Vaccine.

Granulomatous angiitis of the brain. An inflammatory reaction of diverse etiology.

L. Rowland, A. Hays, J. Brust, 1988, Archives of neurology.

Inclusion body myositis mimicking motor neuron disease.

R. Lovelace, W. Trojaborg, L. Rowland, 2001, Archives of neurology.

Antiganglioside antibodies in multifocal acquired sensory and motor neuropathy.

A. Hays, N. Latov, H. Sander, 2003, Archives of neurology.

Anti-sulfatide antibodies in neurological disease: binding to rat dorsal root ganglia neurons

A. Lugaresi, A. Hays, A. Quattrini, 1992, Journal of the Neurological Sciences.

Immune reactive C3d on the surface of myelin sheaths in neuropathy

A. Hays, N. Latov, Sophia S. L. Lee, 1988, Journal of Neuroimmunology.

Motor neuron disease and amyotrophic lateral sclerosis

R. Lovelace, W. Trojaborg, L. Rowland, 1990, Neurology.

Human Monoclonal IgM Anti-Gal(β1-3)GalNAc Autoantibodies Bind to the Surface of Bovine Spinal Motoneurons

L. H. van den Berg, A. Hays, N. Latov, 1990, Journal of neuropathology and experimental neurology.

Tomaculous neuropathy in chromosome 1 Charcot-Marie-Tooth syndrome

G. Rosoklija, R. Lovelace, R. Lebo, 2004, Acta Neuropathologica.

Fragmentation of the Golgi apparatus of motor neurons in amyotrophic lateral sclerosis.

J. Hauw, Z. Mourelatos, N. Gonatas, 1992, The American journal of pathology.

Characteristics of patients with sensory neuropathy diagnosed with abnormal small nerve fibres on skin biopsy

A. Hays, H. Sander, T. Brannagan, 2006, Journal of Neurology, Neurosurgery & Psychiatry.

Amyotrophic lateral sclerosis and neurosarcoidosis: A case report

J. Vonsattel, H. Mitsumoto, A. Hays, 2009, Muscle & nerve.

Expression of HLA-DR in peripheral nerve of amyotrophic lateral sclerosis.

A. Hays, E. Isozaki, A. Gabbai, 1994, Arquivos de neuro-psiquiatria.

A Monoclonal IgA in a Patient with Amyotrophic Lateral Sclerosis Reacts with Neurofilaments and Surface Antigen on Neuroblastoma Cells

L. Rowland, A. Hays, N. Latov, 1990, Journal of neuropathology and experimental neurology.

Complement dependent cytotoxicity of sensory ganglion neurons mediated by the gp120 glycoprotein of HIV-1.

A. Hays, N. Latov, S. Apostolski, 1994, Immunological investigations.

Expression of peripherin in ubiquinated inclusions of amyotrophic lateral sclerosis

A. Hays, C. He, 2004, Journal of the Neurological Sciences.

Increased expression of the pro‐inflammatory enzyme cyclooxygenase‐2 in amyotrophic lateral sclerosis

G. Rosoklija, C. Guégan, S. Przedborski, 2001, Annals of neurology.

Etanercept (Enbrel®) therapy for chronic inflammatory demyelinating polyneuropathy

A. Hays, N. Latov, H. Sander, 2003, Journal of the Neurological Sciences.

Etanercept (EnbrelR) therapy for chronic inflammatory demyelinating polyneuropathy

A. Hays, N. Latov, H. Sander, 2003 .

Experimental demyelination of nerve induced by serum of patients with neuropathy and an anti‐MAG IgM M‐protein

A. Hays, N. Latov, M. Takatsu, 1987, Neurology.

Immunofluorescence study of patients with neuropathy and IgM M proteins

R. Nemni, A. Hays, N. Latov, 1985, Annals of neurology.

Immunocytochemical studies of human peripheral nerve with serum from patients with polyneuropathy and paraproteinemia

E. Zimmerman, A. Hays, N. Latov, 1982, Neurology.

Muscle phosphofructokinase deficiency

M. Hallett, S. Dimauro, A. Hays, 1981, Neurology.

Myoadenylate deaminase deficiency Muscle biopsy and muscle culture in a patient with gout

S. Dimauro, A. Hays, G. Hoffman, 1980, Journal of the Neurological Sciences.

Normal and dystrophin-deficient muscle fibers in carriers of the gene for Duchenne muscular dystrophy.

E. Ricci, S. Servidei, A. Hays, 1988, The American journal of pathology.

Emery‐dreifuss muscular dystrophy

L. Rowland, A. Hays, M. Olarte, 1979, Annals of neurology.

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)

S. Dimauro, L. Salberg, R. Lovelace, 1994, Neurology.

ALTERED SUBICULAR MAP 2 IMMUNOREACTIVITY IN SCHIZOPHRENIA

G. Rosoklija, A. Dwork, J. Keilp, 2006 .

Glycation inactivation of the complement regulatory protein CD59: a possible role in the pathogenesis of the vascular complications of human diabetes.

A. Hays, J. Halperin, M. Chorev, 2004, Diabetes.

Erratum: Polymorphisms in the human apolipoprotein-J/clusterin gene: Ethnic variation and distribution in Alzheimer's disease (Human Genetics (1996) 98 (430-436))

B. Tycko, R. Mayeux, Y. Stern, 1998 .

Electrophysiologic study of experimental demyelination induced by serum of patients with IgM M proteins and neuropathy

R. Lovelace, W. Trojaborg, A. Hays, 1989, Neurology.

Eosinophilic fasciitis associated with the eosinophilia-myalgia syndrome.

A. Hays, I. Jaffe, R. Kopelman, 1990, The American journal of medicine.

Identification of Gal(β1–3)GalNAc bearing glycoproteins at the nodes of ranvier in peripheral nerve

E. Ruoslahti, A. Hays, M. Corbo, 1994, Journal of neuroscience research.

Amyotrophic lateral sclerosis with ragged-red fibers.

S. Dimauro, C. Angelini, H. Mitsumoto, 2008, Archives of neurology.

RAPID COMMUNICATION Immunocytochemical Study of Dystrophin in Muscle Culturesfrom Patients with Duchenne Muscular Dystrophy and Unaffected Control Patients

S. Dimauro, A. Hays, C. Moraes, 2022 .

Apoptosis and Cell Proliferation in Proliferative Retinal Disorders: PCNA, Ki-67, Caspase-3, and PARP Expression

A. Hays, G. Barile, Stanley Chang, 2005, Current eye research.

Peripheral neuropathy and anti-MAG antibodies.

A. Hays, N. Latov, W. Sherman, 1988, Critical reviews in neurobiology.

Maternally inherited cardiomyopathy: an atypical presentation of the mtDNA 12S rRNA gene A1555G mutation.

S. Dimauro, F. Santorelli, C. Casali, 1999, American journal of human genetics.

Creatine kinase isoenzyme transitions in muscle grafts of mice.

A. Hays, A. Miranda, F. Mong, 1982, Cell differentiation.

Benign course of glycogen storage disease type IIb in two brothers: Nature or nurture?

S. Dimauro, S. Tsujino, A. Hays, 2006, Muscle & nerve.

Collagen nerve protector in rat sciatic nerve repair: A morphometric and histological analysis

Paul D. Kim, M. Rosenwasser, A. Hays, 2010, Microsurgery.

Immunocytochemical analysis of normal and acid maltase-deficient muscle cultures.

S. Dimauro, A. Hays, A. Miranda, 1985, Archives of neurology.

Anti‐Hu‐associated peripheral nerve and muscle microvasculitis

G. Inghirami, J. Dalmau, A. Hays, 1994, Neurology.

Axonal neuropathy in eosinophilia–myalgia syndrome

A. Hays, D. Lange, I. Jaffe, 1994, Muscle & nerve.

Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiency.

S. Dimauro, A. Hays, D. Devivo, 1981, Transactions of the American Neurological Association.

Vasculitic neuropathy in a patient with cryoglobulinemia and anti‐MAG IGM monoclonal gammopathy

R. Lovelace, A. Hays, N. Latov, 1992, Muscle & nerve.

Symmetric sarcoid polyneuropathy

R. Nemni, A. Hays, E. T. Gamboa, 1981, Neurology.

Monoclonal IgMK antibody precipitating with chondroitin sulfate C from patients with axonal polyneuropathy and epidermolysis

A. Hays, N. Latov, R. Nemni, 1983, Neurology.

Erroneous diagnosis corrected after 28 years. Not spinal muscular atrophy with ophthalmoplegia but minicore myopathy.

R. Lovelace, R. Rosenberg, P. Gordon, 1996, Archives of Neurology.

X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1.

K. Wilhelmsen, S. Barral, L. Rowland, 2008, American journal of human genetics.

B cell small lymphocytic lymphoma and chronic lymphocytic leukemia with peripheral neuropathy: two cases with neuropathological findings and lymphocyte marker analysis

A. Hays, N. Latov, D. Knowles, 2004, Acta Neuropathologica.

Neurolymphomatosis

R. Lovelace, G. Inghirami, R. Diaz-Arrastia, 1992, Neurology.

Muscle phosphoglycerate rnutase deficiency

S. Dimauro, A. Hays, A. Miranda, 1982, Neurology.

Specificity of mouse and human monoclonal antibodies to myelin‐associated glycoprotein

M. Shy, A. Hays, N. Latov, 1984, Neurology.

Nystagmus in motor neuron disease: Clinicopathological study of two cases

B. Frame, L. Rowland, A. Hays, 1984, Annals of neurology.

Becker muscular dystrophy or spinal muscular atrophy?—Dystrophin studies resolve conflicting results of electromyography and muscle biopsy

R. Lovelace, C. Minetti, A. Hays, 1991, Neuromuscular Disorders.

Adult-onset nemaline myopathy and monoclonal gammopathy.

G. Bhagat, A. Beggs, C. Keller, 2006, Archives of neurology.

Nemaline myopathy: a possible late complication of Hodgkin's disease therapy.

C. Antonescu, M. Rosenblum, P. Boland, 2003, Human pathology.

Duchenne muscular dystrophy: Deficiency of dystrophin at the muscle cell surface

S. Dimauro, L. Kunkel, E. Hoffman, 1988, Cell.

Long‐duration polyphasic motor unit potentials in myopathies: A quantitative study with pathological correlation

R. Lovelace, A. Hays, A. Uncini, 1990, Muscle & nerve.

Myopathy with tubulin-reactive crystalline inclusions

S. Dimauro, A. Hays, E. Bonilla, 2001, Neurology.

Recruitment of the Mitochondrial-Dependent Apoptotic Pathway in Amyotrophic Lateral Sclerosis

G. Rosoklija, M. Vila, C. Guégan, 2001, The Journal of Neuroscience.

Plasma exchange treatment of peripheral neuropathy associated with plasma cell dyscrasia.

A. Hays, N. Latov, W. Sherman, 1984, Journal of neurology, neurosurgery, and psychiatry.

Fatal infantile neuromuscular presentation of glycogen storage disease type IV

W. Chung, S. Dimauro, F. Muntoni, 2004, Neuromuscular Disorders.

Fast muscle fibers are preferentially affected in Duchenne muscular dystrophy

H. Blau, A. Hays, C. Webster, 1988, Cell.

Primary central nervous system lymphoma in childhood presenting as progressive panhypopituitarism.

A. Hays, J. Garvin, N. Feldstein, 2001, Journal of pediatric hematology/oncology.

Lamina-associated polypeptide-1 interacts with the muscular dystrophy protein emerin and is essential for skeletal muscle maintenance.

P. Schulze, W. Dauer, H. Worman, 2013, Developmental cell.

Chromosome 12‐linked autosomal dominant scapuloperoneal muscular dystrophy

T. Gilliam, K. Wilhelmsen, M. Neystat, 1996, Annals of neurology.

Gene expression profiling in chronic inflammatory demyelinating polyneuropathy

M. Dalakas, A. Hays, N. Latov, 2005, Journal of Neuroimmunology.

Polyglucosan body disease

S. Dimauro, R. Lovelace, L. Rowland, 1991, Muscle & nerve.

The role of quantitative electromyography in inclusion body myositis

W. Trojaborg, A. Hays, T. Brannagan, 1997, Journal of neurology, neurosurgery, and psychiatry.

Sensory CIDP presenting as cryptogenic sensory polyneuropathy

S. Croul, A. Hays, N. Latov, 2004, Journal of the peripheral nervous system : JPNS.

Structural abnormalities of subicular dendrites in subjects with schizophrenia and mood disorders: preliminary findings.

G. Rosoklija, A. Dwork, J. Mann, 2000, Archives of general psychiatry.

Absence of echovirus sequences in brain and spinal cord of amyotrophic lateral sclerosis patients

Robert Schlaberg, R. Bowser, A. Hays, 2001, Annals of neurology.

Early-onset toe walking in rippling muscle disease due to a new caveolin-3 gene mutation

C. Kubisch, A. Hays, R. Madrid, 2005, Neurology.

Small-fiber neuropathy/neuronopathy associated with celiac disease: skin biopsy findings.

S. Chin, A. Hays, N. Latov, 2005, Archives of neurology.

Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: A study of 56 patients

S. Dimauro, A. Pestronk, R. Griggs, 1996, Annals of neurology.

Primary melanocytomas of the spinal cord: a report of seven cases.

H. Hibshoosh, A. Hays, C. Baker, 1997, Clinical neuropathology.

134 FOCAL DEMYELINATION OF CAT SCIATIC NERVE INDUCED BY INTRANEURAL INJECTION OF SERUM FROM PATIENTS WITH POLYNEUROPATHY AND MONOCLONAL IgM REACTIVE WITH MYELINASSOCIATED GLYCOPROTEIN

A. Hays, N. Latov, M. Takatsu, 1983 .

Polyneuropathy in nonmalignant IgM plasma cell dyscrasia: a morphological study.

A. Hays, N. Latov, R. Nemni, 1983, Annals of neurology.

Reduction of a 4q35-encoded nuclear envelope protein in muscle differentiation.

E. C. Schirmer, H. Worman, A. Hays, 2009, Biochemical and biophysical research communications.

Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactions.

K. Campbell, L. E. Lim, C. Stolle, 2000, Human molecular genetics.

Inducible overexpression of wild-type prion protein in the muscles leads to a primary myopathy in transgenic mice

Ken Chen, Ping Wang, Meiling Wang, 2007, Proceedings of the National Academy of Sciences.

The gp 120 glycoprotein of human immunodeficiency virus type 1 binds to sensory ganglion neurons

G. Rosoklija, S. Levison, S. Lederman, 1993, Annals of neurology.

Polyneuropathy in nonmalignant IgM plasma cell dyscrasia: A Morphological study

A. Hays, N. Latov, R. Nemni, 1983, Annals of neurology.

Autopsy-proven amyotrophic lateral sclerosis, Waldenstrom's macroglobulinemia, and antibodies to sulfated glucuronic acid paragloboside

W. Trojaborg, L. Rowland, A. Hays, 1995, Neurology.

Reply from the Authors

L. Rowland, A. Hays, N. Latov, 1996, Neurology.

Lymphoproliferative disorders and motor neuron disease

R. Lovelace, W. Trojaborg, P. Gordon, 1998, Neurology.

Neuropathy and anti‐MAG antibodies without detectable serum M‐protein

R. Lovelace, L. Rowland, A. Hays, 1984, Neurology.

The natural history of primary lateral sclerosis

H. Mitsumoto, P. Gordon, L. Rowland, 2006, Neurology.

Antibodies to glycoconjugates in human motor neuron disease.

A. Hays, N. Latov, R. Yu, 1988, Neurochemical pathology.

Diagnostic biopsy of the motor nerve to the gracilis muscle. Technical note.

L. Rowland, A. Hays, M. Corbo, 1996, Journal of neurosurgery.

Altered subicular MAP2 immunoreactivity in schizophrenia.

G. Rosoklija, A. Dwork, J. Keilp, 2005, Prilozi.

RAGE modulates peripheral nerve regeneration via recruitment of both inflammatory and axonal outgrowth pathways

W. Trojaborg, A. Schmidt, T. Wendt, 2004, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Local activation of the complement system in endoneurial microvessels of diabetic neuropathy

G. Rosoklija, A. Dwork, A. Hays, 2000, Acta Neuropathologica.

Respiratory distress as the initial manifestation of Werdnig-Hoffmann disease.

R. Mellins, W. Berdon, A. Hays, 1974, Pediatrics.

A prospective cohort study of neuropsychological test performance in ALS

K. Marder, Y. Stern, R. Goetz, 2010, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Intracranial dissecting aneurysms in childhood.

R. Nass, A. Hays, A. Chutorian, 1982, Stroke.

Brain Tissue Heterotopia in the Eighth Cranial Nerve

J. Wazen, H. Silverstein, A. Hays, 1987, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

ANTISULFATIDE ANTIBODIES IN NEUROPATHY—CLINICAL AND ELECTROPHYSIOLOGIC CORRELATES

A. Hays, N. Latov, R. Dabby, 2000 .

Poststroke depression and emotional incontinence

A. Hays, N. Latov, R. Dabby, 2000, Neurology.

Celiac neuropathy

A. Hays, N. Latov, H. Sander, 2003, Neurology.

Recurrent transient monocular visual impairment caused by hyphema following intraocular surgery

A. Hays, D. Devivo, J. Garvin, 1988, Neurology.

Identification of a novel mutation in the mtDNA ND5 gene associated with MELAS.

S. Dimauro, F. Santorelli, L. Vilarinho, 1997, Biochemical and biophysical research communications.

Cytochrome c oxidase deficiency due to a novel SCO2 mutation mimics Werdnig-Hoffmann disease.

S. Dimauro, E. Schon, P. Canoll, 2002, Archives of neurology.

A benign motor neuron disorder: Delayed cramps and fasciculation after poliomyelitis or myelitis

R. Lovelace, L. Rowland, A. Hays, 1982, Annals of neurology.

LIPID MYOPATHY AND CONGENITAL ICHTHYOSIS-A NEW DISORDER, PROBABLY GENETIC: 94

S. Dimauro, R. Mayeux, W. Johnson, 1976 .

Diagnostic biopsy of the motor nerve to the gracilis muscle: Clinical pearl

L. Rowland, A. Hays, M. Corbo, 1996 .

Amyotrophic lateral sclerosis with multiple sclerosis: A clinical and pathological report

S. Staugaitis, H. Mitsumoto, A. Hays, 2000, Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases.

Induction of human IgM and IgG anti-GM1 antibodies in transgenic mice in response to lipopolysaccharides from Campylobacter jejuni

H. Willison, A. Hays, N. Latov, 2004, Journal of Neuroimmunology.

Peripheral nerve immunohistochemistry in diabetic neuropathy.

G. Rosoklija, A. Hays, D. Younger, 1996, Seminars in neurology.

Expression of a cell death marker (Clusterin) in muscle target fibers.

G. Duigou, A. Hays, M. Corbo, 1993, Arquivos de neuro-psiquiatria.

Muscle carnitine deficiency Genetic heterogeneity

S. Dimauro, R. Lovelace, A. Hays, 1979, Journal of the Neurological Sciences.

Quantitative objective markers for upper and lower motor neuron dysfunction in ALS

S L Pullman, J. Hirsch, J. Hirsch, 2007, Neurology.

Human immunodeficiency virus infection of dorsal root ganglion neurons detected by polymerase chain reaction in situ hybridization

G. Nuovo, A. Hays, N. Latov, 1997, Annals of neurology.