M. Patterson

M. Patterson, M. Pineda, C. Gama, 2019, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

Stable or improved neurological manifestations during miglustat therapy in patients from the international disease registry for Niemann-Pick disease type C: an observational cohort study

M. Patterson, M. Pineda, M. Vanier, 2015, Orphanet Journal of Rare Diseases.

The Niemann-Pick Disease Type C Suspicion Index: Development of a New Tool to Aid Diagnosis

M. Patterson, M. Walterfang, H. Runz, 2015 .

Genetic screening for Niemann–Pick disease type C in adults with neurological and psychiatric symptoms: findings from the ZOOM study

D. Balding, D. Linden, P. Bauer, 2013, Human molecular genetics.

Niemann-Pick type C Suspicion Index tool: analyses by age and association of manifestations

F. Sedel, M. Patterson, M. Walterfang, 2013, Journal of Inherited Metabolic Disease.

Disease and patient characteristics in NP-C patients: findings from an international disease registry

M. Patterson, M. Pineda, M. Vanier, 2013, Orphanet Journal of Rare Diseases.

Miglustat in adult and juvenile patients with Niemann-Pick disease type C: long-term data from a clinical trial.

M. Patterson, J. E. Wraith, L. Abel, 2010, Molecular genetics and metabolism.

The effect of cholesterol‐lowering agents on hepatic and plasma cholesterol in Niemann‐Pick disease type C

R. Schiffmann, M. Patterson, R. Brady, 1993, Neurology.

Biochemical and clinical response after umbilical cord blood transplant in a boy with early childhood‐onset beta‐mannosidosis

M. Patterson, J. Eisengart, P. Orchard, 2019, Molecular genetics & genomic medicine.

Linkage of Niemann-Pick disease type C to human chromosome 18.

M. Polymeropoulos, R. Straub, S. Detera-Wadleigh, 1993, Proceedings of the National Academy of Sciences of the United States of America.

Spiral analysis in Niemann‐Pick disease type C

M. Patterson, S. Pullman, A. Floyd, 2009, Movement disorders : official journal of the Movement Disorder Society.

39 – Diseases Associated with Primary Abnormalities in Carbohydrate Metabolism

M. Patterson, 2017 .

JIMD Reports, Volume 40

M. Baumgartner, M. Patterson, S. Rahman, 2018, JIMD Reports.

Progesterone blocks cholesterol translocation from lysosomes.

M. Patterson, S. Patel, E. Goldin, 1992, The Journal of biological chemistry.

Niemann–Pick Disease

M. Patterson, 2017 .

Abetalipoproteinemia (ABL, Bassen–Kornzweig Disease)

M. Patterson, 2003 .

JIMD Reports, Volume 25

M. Baumgartner, M. Patterson, S. Rahman, 2016, JIMD Reports.

Should patients with Phosphomannomutase 2-CDG (PMM2-CDG) be screened for adrenal insufficiency?

M. Patterson, H. Plotkin, Christina Lam, 2021, Molecular genetics and metabolism.

Case definition and classification of leukodystrophies and leukoencephalopathies.

F. Eichler, A. Vanderver, R. Schiffmann, 2015, Molecular genetics and metabolism.

Angelman's syndrome: clinical and electroencephalographic findings.

M. Patterson, B. Westmoreland, D. Rubin, 1997, Electroencephalography and clinical neurophysiology.

The US Network of Pediatric Multiple Sclerosis Centers

E. Waubant, M. Patterson, Moses Rodriguez, 2015, Journal of child neurology.

The frequency of non-epileptic spells in children: Results of video–EEG monitoring in a tertiary care center

M. Patterson, J. Cappell, C. Chiriboga, 2008, Seizure.

Functional significance of PMM2 mutations in mildly affected patients with congenital disorders of glycosylation Ia

H. Freeze, M. Patterson, E. Treacy, 2001, Genetics in Medicine.

Violent recurrent ballism associated with infections in two children with static encephalopathy

M. Patterson, M. Zupanc, J. Ahlskog, 2000, Movement disorders : official journal of the Movement Disorder Society.

International clinical guidelines for the management of phosphomannomutase 2‐congenital disorders of glycosylation: Diagnosis, treatment and follow up

H. Freeze, M. Patterson, Christina Lam, 2019, Journal of inherited metabolic disease.

Fabry's Disease

M. Patterson, 2003 .

Quo vadis now: Beyond genomics to an era of personalised medicine

M. Baumgartner, M. Patterson, S. Rahman, 2022, Journal of inherited metabolic disease.

Mosaicism of the UDP-galactose transporter SLC35A2 causes a congenital disorder of glycosylation.

Emily H Turner, J. Shendure, D. Nickerson, 2013, American journal of human genetics.

De Novo DNM1L Variant in a Teenager With Progressive Paroxysmal Dystonia and Lethal Super-refractory Myoclonic Status Epilepticus

E. Wirrell, M. Patterson, D. Babovic‐Vuksanovic, 2018, Journal of child neurology.

The murine Niemann-Pick type C lesion affects testosterone production.

M. Patterson, R. Brady, J. Strauss, 1993, Endocrinology.

Metabolic mimics: the disorders of N-linked glycosylation.

M. Patterson, 2005, Seminars in pediatric neurology.

Role for protein kinase C in A23187 induced glomerular arachidonate release and PGE2 production.

M. Patterson, F. DeRubertis, P. Craven, 1987, Biochemical and biophysical research communications.

Quo vadis: the re-definition of “inborn metabolic diseases”

M. Baumgartner, M. Patterson, S. Rahman, 2015, Journal of Inherited Metabolic Disease.

Clinical, Radiologic, and Prognostic Features of Myelitis Associated With Myelin Oligodendrocyte Glycoprotein Autoantibody

K. Tyler, B. Weinshenker, M. Patterson, 2019, JAMA neurology.

Childhood dural arteriovenous fistulae of the posterior dural sinuses: three case reports and literature review.

D. Nichols, F. Meyer, M. Patterson, 1995, Neurosurgery.

Role of Enhanced Arachidonate Availability Through Phospholipase A2 Pathway in Mediation of Increased Prostaglandin Synthesis by Glomeruli From Diabetic Rats

M. Patterson, F. DeRubertis, P. Craven, 1988, Diabetes.

Mutation causing congenital myasthenia reveals acetylcholine receptor beta/delta subunit interaction essential for assembly.

K. Ohno, M. Patterson, S. Sine, 1999, The Journal of clinical investigation.

Disease specific therapies in leukodystrophies and leukoencephalopathies.

F. Eichler, A. Vanderver, R. Schiffmann, 2015, Molecular genetics and metabolism.

From stargazing chicks to seizing infants

M. Patterson, 2009, Neurology.

Lost in translation—Challenges in drug development for inherited metabolic diseases

M. Patterson, R. Lachmann, S. Sirrs, 2022, Journal of inherited metabolic disease.

Contrasting effects of IFNβ and IVIG in children with central and peripheral demyelination

B. Weinshenker, M. Patterson, M. Rodríguez, 2003, Neurology.

Linear clinical progression, independent of age of onset, in Niemann–Pick disease, type C

W. Pavan, M. Patterson, C. Brewer, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Niemann-Pick disease, type C and Roscoe Brady.

M. Patterson, S. Walkley, 2017, Molecular genetics and metabolism.

An intracranial arteriovenous malformation and palatal myoclonus related to pseudoxanthoma elasticum.

J. Chalk, M. Patterson, M. Pender, 1989, Australian and New Zealand journal of medicine.

Niemann-Pick C1 disease gene: homology to mediators of cholesterol homeostasis.

K. G. Coleman, M. Polymeropoulos, W. Pavan, 1997, Science.

Scurvy and Rickets Masked by Chronic Neurologic Illness: Revisiting “Psychologic Malnutrition”

M. Patterson, J. Noble, Arthur M. Mandel, 2007, Pediatrics.

JIMD Reports, Volume 41: Focus Issue: Adults and Metabolism

M. Baumgartner, M. Patterson, S. Rahman, 2018, JIMD Reports.

JIMD Reports, Volume 36

M. Baumgartner, M. Patterson, S. Rahman, 2017, JIMD Reports.

An international classification of inherited metabolic disorders (ICIMD)

Robert W. Taylor, A. Ballabio, E. Bertini, 2020, Journal of inherited metabolic disease.

JIMD Reports, Volume 26

M. Baumgartner, M. Patterson, S. Rahman, 2016, JIMD Reports.

Jeavons Syndrome: Clinical Features and Response to Treatment.

J. Britton, G. Cascino, E. Wirrell, 2018, Pediatric neurology.

The long-term outcomes of presymptomatic infants transplanted for Krabbe disease: Report of the workshop held on July 11 and 12, 2008, Holiday Valley, New York

V. Caviness, M. Patterson, C. Whitley, 2009, Genetics in Medicine.

Fetal Transplantation for Huntington’s Disease: Clinical Studies

M. Patterson, L. Philpott, S. Jacques, 1998 .

Isolated horizontal supranuclear gaze palsy as a marker of severe systemic involvement in Gaucher's disease

M. Patterson, R. Brady, J. Higgins, 1993, Neurology.

Miglustat in Niemann-Pick disease type C patients: a review

M. Patterson, M. Walterfang, M. Pineda, 2018, Orphanet Journal of Rare Diseases.

Recommendations for the detection and diagnosis of Niemann-Pick disease type C

P. Bauer, M. Patterson, M. Strupp, 2017, Neurology. Clinical practice.

Recommendations for the diagnosis and management of Niemann-Pick disease type C: an update.

F. Sedel, M. Patterson, M. Walterfang, 2012, Molecular genetics and metabolism.

Therapy of Niemann-Pick disease, type C.

M. Patterson, F. Platt, 2004, Biochimica et biophysica acta.

Mutation causing congenital myasthenia reveals acetylcholine receptor β/δ subunit interaction essential for assembly

K. Ohno, M. Patterson, S. Sine, 1999 .

JIMD Reports, Volume 45

M. Baumgartner, M. Patterson, S. Rahman, 2019, JIMD Reports.

Research challenges in central nervous system manifestations of inborn errors of metabolism.

J. Mink, J. Provenzale, M. Patterson, 2011, Molecular genetics and metabolism.

The Eight and a Half Year Journey of Undiagnosed AD: Gene Sequencing and Funding of Advanced Genetic Testing Has Led to Hope and New Beginnings

M. Patterson, R. Kooy, A. van Dijck, 2017, Front. Endocrinol..

JIMD Reports, Volume 43

M. Baumgartner, M. Patterson, S. Rahman, 2019, JIMD Reports.

Posterior reversible encephalopathy syndrome and hemorrhage associated with tacrolimus in a pediatric heart transplantation recipient

M. Patterson, D. Driscoll, P. O’Leary, 2013, Pediatric transplantation.

Expanded genetic insight and clinical experience of DNMT1-complex disorder

David T. Jones, J. Graff‐Radford, K. Maski, 2020, Neurology: Genetics.

Severe hypoglycemia as a presenting symptom of carbohydrate-deficient glycoprotein syndrome.

H. Freeze, M. Patterson, J. Vockley, 1999, The Journal of pediatrics.

JIMD Reports, Volume 39

M. Patterson, S. Rahman, J. Zschocke, 2018, JIMD Reports.

Neurological aspects of human glycosylation disorders.

H. Freeze, E. Eklund, M. Patterson, 2015, Annual review of neuroscience.

JIMD Reports, Volume 23

M. Baumgartner, M. Patterson, S. Rahman, 2015 .

Neurological Complications of Measles (Rubeola)

M. Patterson, 2020, Current Neurology and Neuroscience Reports.

Acetylcholine receptor beta-subunit mutations causing endplate AChR deficiency and reduced assembly with the delta subunit

K. Ohno, M. Patterson, S. Sine, 1999 .

Pompe disease diagnosis and management guideline

David M. Rapoport, Michael S. Watson, Robert D. Steiner, 2006, Genetics in Medicine.

Functional characterization of a GFAP variant of uncertain significance in an Alexander disease case within the setting of an individualized medicine clinic

Michael T. Zimmermann, M. Patterson, M. Zimmermann, 2016, Clinical case reports.

KCNQ2 encephalopathy

Eric Marsh, Brenda Porter, Vinodh Narayanan, 2016, Neurology: Genetics.

Neurotransmitter Abnormalities and Response to Supplementation in Spg11 Nih Public Access Author Manuscript

Rena A. Godfrey, A. Vanderver, M. Patterson, 2022 .

Whole-Exome Sequencing in the Clinic: Lessons from Six Consecutive Cases from the Clinician's Perspective

M. Patterson, S. Kirmani, B. Wical, 2015, Molecular Syndromology.

Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration (HARP syndrome)

M. Patterson, R. Brady, J. Higgins, 1992, Neurology.

A clinical approach to the diagnosis of patients with leukodystrophies and genetic leukoencephelopathies.

Ryan J Taft, Adeline Vanderver, Geneviève Bernard, 2015, Molecular genetics and metabolism.

Consensus statement on preventive and symptomatic care of leukodystrophy patients.

A. Vanderver, M. Patterson, J. Bonkowsky, 2015, Molecular genetics and metabolism.

Proton Magnetic Resonance Spectroscopy as a Probe into the Pathophysiology of Autism Spectrum Disorders (ASD): A Review

J. Port, M. Patterson, C. Wall, 2013, Autism research : official journal of the International Society for Autism Research.

SLC35A2‐CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported Individuals

J. Rosenfeld, I. Scheffer, S. Nelson, 2019, Human mutation.

Cerebellar leukoencephalopathy

W. Arts, C. Gomez, M. Patterson, 2008, Neurology.

Limbic encephalitis associated with anti‐GAD antibody and common variable immune deficiency

M. Patterson, Ç. Akman, A. Rubinstein, 2009, Developmental medicine and child neurology.

Free sialic acid storage disorder: Progress and promise

M. Lek, R. Zoncu, M. Patterson, 2021, Neuroscience Letters.

Dolichol phosphate mannose synthase (DPM1) mutations define congenital disorder of glycosylation Ie (CDG-Ie)

H. Freeze, M. Patterson, G. Srikrishna, 2000, The Journal of clinical investigation.

Identification of 58 novel mutations in Niemann‐Pick disease type C: Correlation with biochemical phenotype and importance of PTC1‐like domains in NPC1

Karen Snow, M. Patterson, P. Lundquist, 2003, Human mutation.

The pathophysiology and mechanisms of NP-C disease.

M. Patterson, W. Balch, S. Sturley, 2004, Biochimica et biophysica acta.

JIMD Reports, Volume 44

M. Baumgartner, M. Patterson, S. Rahman, 2019, JIMD Reports.

Secondary Narcolepsy in Children

M. Patterson, S. Kotagal, G. Keating, 2020, Journal of child neurology.

Hematopoietic cell transplantation for sialidosis type I

M. Patterson, J. Eisengart, P. Orchard, 2021, Molecular genetics and metabolism reports.

Loss of the sphingolipid desaturase DEGS1 causes hypomyelinating leukodystrophy

Kiely N. James, A. Fatemi, M. Tarnopolsky, 2019, The Journal of clinical investigation.

JIMD Reports, Volume 38

M. Patterson, S. Rahman, 2018, JIMD Reports.

Genomic organization of the human phosphomannose isomerase (MPI) gene and mutation analysis in patients with congenital disorders of glycosylation type Ib (CDG‐Ib)

H. Freeze, M. Patterson, G. Matthijs, 2000, Human mutation.

Successful treatment of intrathecal methotrexate overdose by using ventriculolumbar perfusion and intrathecal instillation of carboxypeptidase G2.

M. Patterson, P. Adamson, B. Widemann, 1996, Mayo Clinic proceedings.

Editorial comment: Ataxia, ophthalmoplegia, and impairment of consciousness in a 19 month-old American boy.

M. Patterson, 2014, Seminars in pediatric neurology.

Impacts and Burden of Niemann pick Type-C: a patient and caregiver perspective

M. Patterson, T. Symonds, E. Mengel, 2021, Orphanet Journal of Rare Diseases.

Clinical disease characteristics of patients with Niemann-Pick Disease Type C: findings from the International Niemann-Pick Disease Registry (INPDR)

M. Patterson, B. Bembi, P. Gissen, 2021, Orphanet Journal of Rare Diseases.

Efficacy and safety of arimoclomol in Niemann‐Pick disease type C: Results from a double‐blind, randomised, placebo‐controlled, multinational phase 2/3 trial of a novel treatment

M. Patterson, R. D. Da Riol, M. Gautschi, 2021, Journal of inherited metabolic disease.

Validation of a short-form 5-domain Niemann-Pick type C clinical severity scale (5-domain NPCCSS)

Tara Symonds, Stacie Hudgens, Marc Patterson, 2021 .

Efficacy and safety of arimoclomol in patients with Niemann-Pick disease type C: Results from a double-blind, randomized placebo-controlled trial with a novel treatment

M. Patterson, B. Bembi, M. Gautschi, 2020 .

Assessment of the immunogenic potential of Rhodococcus equi virulence associated protein (VapA) in mice.

M. Patterson, J. Prescott, J. Yager, 1997, Veterinary microbiology.

Use of Rhodococcus equi virulence-associated protein for immunization of foals against R equi pneumonia.

M. Patterson, J. Prescott, M. Holmes, 1997, American journal of veterinary research.

Editorial comment: Cerebellar ataxia, vertical supranuclear gaze palsy, sensorineural deafness, epilepsy, dementia and hallucinations in an adolescent male.

M. Patterson, 2014, Seminars in pediatric neurology.

Oculomotor and Vestibular Findings in Gaucher Disease Type 3 and Their Correlation with Neurological Findings

R. Strobl, R. Schiffmann, M. Patterson, 2018, Front. Neurol..

Severe Hajdu-Cheney syndrome with upper airway obstruction.

M. Patterson, V. Michels, P. A. Crifasi, 1997, American journal of medical genetics.

Views of Recently First-Certified US Child Neurologists on Their Residency Training

M. Patterson, D. Gilbert, I. Valencia, 2013, Journal of child neurology.

LGI1 and CASPR2 neurological autoimmunity in children

Amanda L. Piquet, E. Wirrell, M. Patterson, 2018, Annals of neurology.

Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b gene

S. Dimauro, J. Stevens, M. Mancuso, 2003, Journal of the Neurological Sciences.

Pompe disease diagnosis and management guideline ACMG Work Group on Management of Pompe Disease :

B. Byrne, D. Rapoport, M. Watson, 2006 .

Congenital disorders of N-linked glycosylation

M. Patterson, 2020, Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease.

40 – Disorders of Glycosylation

H. Freeze, M. Patterson, B. Ng, 2017 .

Teaching NeuroImages: Call it as you see it

M. Patterson, E. Coon, 2012, Neurology.

Myelination disturbance in a patient with hyperuricemia and hyperserotoninemia combined with 18q deletion syndrome.

M. Patterson, E. Vörös, A. László, 2009, Ideggyogyaszati szemle.

Features , mutational hot spots , and ezogabine treatment of 11 patients

L. Carmant, V. Narayanan, M. Patterson, 2022 .

Acute Encephalopathy With Biphasic Seizures and Late Restricted Diffusion.

M. Patterson, M. Ruff, E. Hoffman, 2016, Pediatric neurology.

Rectal Biopsy in the Diagnosis of Neuronal Intranuclear Hyaline Inclusion Disease

M. Patterson, S. Chin, R. Kairam, 2004, Journal of child neurology.

Movers and shakers

M. Patterson, 2010, Neurology.

The More Things Change… Child Neurology in the Age of Next-Generation Sequencing.

M. Patterson, 2017, Seminars in pediatric neurology.

Cognitive Impairment Occurs in Children and Adolescents With Multiple Sclerosis

E. Waubant, R. Benedict, M. Patterson, 2013, Journal of child neurology.

Massive expansion of SCA2 with autonomic dysfunction, retinitis pigmentosa, and infantile spasms

C. Gomez, M. Patterson, C. Gomez, 2011, Neurology.

Kinematic analysis of motor dysfunction in Niemann-Pick type C

M. Patterson, S. Pullman, Q. Yu, 2007, Clinical Neurophysiology.

Further delineation of the phenotypic spectrum associated with hemizygous loss‐of‐function variants in NONO

J. Rosenfeld, M. Patterson, Yaping Yang, 2019, American journal of medical genetics. Part A.

JIMD Reports, Volume 30

M. Baumgartner, M. Patterson, S. Rahman, 2016, JIMD Reports.

Subclinical seizures in children diagnosed with localization-related epilepsy: Clinical and EEG characteristics

M. Patterson, C. Chiriboga, M. Montenegro, 2009, Epilepsy & Behavior.

Spontaneous improvement of carbohydrate-deficient transferrin in PMM2-CDG without mannose observed in CDG natural history study

H. Freeze, M. Patterson, Christina Lam, 2021, Orphanet Journal of Rare Diseases.

Guidelines in the JIMD: Evidence‐based practice for inherited metabolic disease

M. Baumgartner, M. Patterson, S. Rahman, 2023, Journal of inherited metabolic disease.

RESPONSE TO IMMUNOTHERAPY IN A 20-MONTH-OLD BOY WITH ANTI-NMDA RECEPTOR ENCEPHALITIS

M. Patterson, J. Dalmau, L. Wong-Kisiel, 2010, Neurology.

Rapidly Progressive Paraplegia in an 11-Year-Old Girl: A Case of Spinal Cord Infarction and Expected Imaging Findings

M. Patterson, W. Edlund, A. Hewitt, 2020, Child neurology open.

JIMD Reports, Volume 20

M. Baumgartner, M. Patterson, S. Rahman, 2015 .

Cerebral and cerebellar white matter abnormalities with magnetic resonance imaging in a child with Feingold syndrome

M. Patterson, D. Babovic‐Vuksanovic, C. Rydberg, 2009, American Journal of Medical Genetics. Part A.

Erratum: Pompe disease diagnosis and management guidelines (Genetics in Medicine (May 2006) 8 (267-288))

B. Byrne, D. Rapoport, M. Watson, 2006 .

IGF system in children with congenital disorders of glycosylation

M. Patterson, C. Conover, B. Miller, 2009, Clinical endocrinology.

Co-morbidity of Sanfilippo Syndrome type C and d-2-hydroxyglutaric aciduria

M. Patterson, S. Kirmani, D. Oglesbee, 2011, Journal of Neurology.

111. Miglustat in Niemann-Pick disease type C (NPC)

M. Patterson, L. Abel, D. Vecchio, 2008 .

Screening for "Prelysosomal Disorders": Carbohydrate-Deficient Glycoprotein Syndromes

M. Patterson, 1999, Journal of child neurology.

JIMD Reports, Volume 42

M. Baumgartner, M. Patterson, S. Rahman, 2018, JIMD Reports.

Diagnosis of Niemann-Pick disease type C.

M. Patterson, P. Pentchev, 1994, Jornal de Pediatria.

Safety and efficacy of (+)‐epicatechin in subjects with Friedreich's ataxia: A phase II, open‐label, prospective study

M. Patterson, A. Badley, R. Gavrilova, 2020, Journal of inherited metabolic disease.

Mental retardation

H. Zoghbi, M. Patterson, 2003, Neurology.

Holoprosencephaly: the face predicts the brain; the image predicts its function.

M. Patterson, 2002, Neurology.

Too Old for a Diaper! A Child With Diaper Changing-Induced Seizures.

M. Patterson, L. Wong-Kisiel, A. Feyissa, 2016, Pediatric neurology.

Erratum: Movers and shakers: Diagnosing neurotransmitter diseases with CSF (Neurology (2010) 75 (15-17))

M. Patterson, 2010 .

Correction: Disease and patient characteristics in NP-C patients: findings from an international disease registry

M. Patterson, M. Pineda, M. Vanier, 2013, Orphanet Journal of Rare Diseases.

Movement and Allied Disorders in Childhood

M. Patterson, 1997 .

JIMD Reports, Volume 18

M. Baumgartner, M. Patterson, S. Rahman, 2015 .

Teaching NeuroImages: Neuroimaging Findings in Inosine Triphosphate Pyrophosphohydrolase Deficiency

M. Patterson, S. Wortmann, J. Bierau, 2021, Neurology.

Ictus emeticus

M. Patterson, C. Panayiotopoulos, P. Pentchev, 1996, Neurology.

Linear clinical progression, independent of age of onset, in Niemann–Pick disease, type C

W. Pavan, M. Patterson, C. Brewer, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Cognitive Impairment Occurs in Children and Adolescents With Multiple Sclerosis

E. Waubant, R. Benedict, M. Patterson, 2013, Journal of child neurology.

Movers and shakers

M. Patterson, 2010, Neurology.

Challenging dogma: report of a spinal cord arteriovenous malformation as an acquired lesion in a pediatric patient.

M. Patterson, E. Ahn, G. Lanzino, 2019, Journal of neurosurgery. Spine.

Neurotransmitter abnormalities and response to supplementation in SPG11.

Rena A. Godfrey, A. Vanderver, M. Patterson, 2012, Molecular genetics and metabolism.