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Last Name

profilePatricia E. Greenstein, M.D.

TitleAssistant Professor of Neurology
InstitutionBeth Israel Deaconess Medical Center
AddressBeth Israel Deaconess Med Ctr
330 Brookline Ave
Boston MA 02215
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Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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  1. Waisbren SE, Prabhu SP, Greenstein P, Petty C, Schomer D, Anastasoaie V, Charette K, Rodriguez D, Merugumala S, Lin AP. Improved Measurement of Brain Phenylalanine and Tyrosine Related to Neuropsychological Functioning in Phenylketonuria. JIMD Rep. 2017; 34:77-86. PMID: 27677920.
    View in: PubMed
  2. Farzan F, Wu Y, Manor B, Anastasio EM, Lough M, Novak V, Greenstein PE, Pascual-Leone A. Cerebellar TMS in treatment of a patient with cerebellar ataxia: evidence from clinical, biomechanics and neurophysiological assessments. Cerebellum. 2013 Oct; 12(5):707-12. PMID: 23625327; PMCID: PMC3951770.
  3. Zesiewicz TA, Greenstein PE, Sullivan KL, Wecker L, Miller A, Jahan I, Chen R, Perlman SL. A randomized trial of varenicline (Chantix) for the treatment of spinocerebellar ataxia type 3. Neurology. 2012 Feb 21; 78(8):545-50. PMID: 22323747.
    View in: PubMed
  4. Waisbren SE, Potter NL, Gordon CM, Green RC, Greenstein P, Gubbels CS, Rubio-Gozalbo E, Schomer D, Welt C, Anastasoaie V, D'Anna K, Gentile J, Guo CY, Hecht L, Jackson R, Jansma BM, Li Y, Lip V, Miller DT, Murray M, Power L, Quinn N, Rohr F, Shen Y, Skinder-Meredith A, Timmers I, Tunick R, Wessel A, Wu BL, Levy H, Elsas L, Berry GT. The adult galactosemic phenotype. J Inherit Metab Dis. 2012 Mar; 35(2):279-86. PMID: 21779791; PMCID: PMC3641771.
  5. Sengupta S, Pedersen NP, Davis JE, Rojas R, Reddy H, Kasper E, Greenstein P, Wong ET. Illusion of stroke: intravascular lymphomatosis. Rev Neurol Dis. 2011; 8(3-4):e107-13. PMID: 22249564.
    View in: PubMed
  6. Greenstein PE, Vonsattel JP, Margolis RL, Joseph JJ . HDL2 Neuropathology. Movement Disorders, In. 2007; In press.
  7. Greenstein PE. Neurogenetics. Neurology Review for Psychiatrists. Editors: Ronthal MR and Savitz SL. 2007; In press.
  8. Byrnes V, Afdhal N, Challies T, Greenstein PE. Drug induced liver injury secondary to interferon-beta (IFN-beta) in multiple sclerosis. Ann Hepatol. 2006 Jan-Mar; 5(1):56-9. PMID: 16531969.
    View in: PubMed
  9. Margolis RL, Holmes SE, Rosenblatt A, Gourley L, O'Hearn E, Ross CA, Seltzer WK, Walker RH, Ashizawa T, Rasmussen A, Hayden M, Almqvist EW, Harris J, Fahn S, MacDonald ME, Mysore J, Shimohata T, Tsuji S, Potter N, Nakaso K, Adachi Y, Nakashima K, Bird T, Krause A, Greenstein P. Huntington's Disease-like 2 (HDL2) in North America and Japan. Ann Neurol. 2004 Nov; 56(5):670-4. PMID: 15468075.
    View in: PubMed
  10. Greenstein P. The Development of a Neurogenetics Curriculum using MyCourses for HMS students. Academy Day Plenary Session. Harvard Medical School, Boston MA. 2003.
  11. Greenstein PE, Joseph JT and Margolis RL. Genotype-Phenotype Correlations in HDL2. American Academy of Neurology Meetings. San Francisco, CA. 2003.
  12. Greenstein P. Tick paralysis. Med Clin North Am. 2002 Mar; 86(2):441-6. PMID: 11982312.
    View in: PubMed
  13. Greenstein P. Tick Paralysis. The Medical Clinics of North America: Tick Borne Diseases. Editor: Edlow JA. 2002; 441-447.
  14. Karadimas CL, Greenstein P, Sue CM, Joseph JT, Tanji K, Haller RG, Taivassalo T, Davidson MM, Shanske S, Bonilla E, DiMauro S. Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA. Neurology. 2000 Sep 12; 55(5):644-9. PMID: 10980727.
    View in: PubMed
  15. Karadimas CL, Greenstein P, Joseph JT, Bonilla E, Tanji K, Shanske S, Sue SM and Dimauro S. A novel missense mutation in the mtDNA COX1 gene: Another cause of myopathy with myoglobinuria. American Society of Human Genetics Meetings. San Francisco, CA. 1999.
  16. Ronthal M and Greenstein P. Myoclonus and Asterixis. Movement Disorders in Neurology and Psychiatry Editors: Joseph AB, Young RR. 1998; 449-456.
  17. Joseph JT, Richards CS, Anthony DC, Upton M, Perez-Atayde AR, Greenstein P. Congenital myotonic dystrophy pathology and somatic mosaicism. Neurology. 1997 Nov; 49(5):1457-60. PMID: 9371942.
    View in: PubMed
  18. Greenstein PE, Moore D, Levy-Lohad E, Stephens K, Bird TD. Nine families with the SCA3/Machado-Joseph disease type of inherited ataxia. Neurology. 1996 Oct; 47(4):1106-7. PMID: 8857759.
    View in: PubMed
  19. Ekker SC, Ungar AR, Greenstein P, von Kessler DP, Porter JA, Moon RT, Beachy PA. Patterning activities of vertebrate hedgehog proteins in the developing eye and brain. Curr Biol. 1995 Aug 01; 5(8):944-55. PMID: 7583153.
    View in: PubMed
  20. Kelly GM, Greenstein P, Erezyilmaz DF, Moon RT. Zebrafish wnt8 and wnt8b share a common activity but are involved in distinct developmental pathways. Development. 1995 Jun; 121(6):1787-99. PMID: 7600994.
    View in: PubMed
  21. Greenstein P and Bird TD. The New Molecular Biology of Neurological Disease. Focus and Opinion: Internal Medicine. 1995; 3:178-186.
  22. Greenstein P and Bird TD. Neurogenetics: triumphs and Challenges. Western Journal of Medicine. 1995; 161(3):242-246.
  23. Greenstein P, Levy-Lahad E, Ranum, L and Bird, TD. Remarkable phenotypic heterogeneity in two families with non-Portuguese Machado Joseph Disease. World Federation Meetings of Neurogenetics. Seattle, WA. 1995.
  24. Kelly GM, Greenstein P, Erezylimas DF and Moon RT. Expression of wnt8 and wnt8b during zebrafish embryogenesis. Zebrafish Development and Genetics Meetings, Cold Spring Harbor Labs, Long Island, NY. 1994.
  25. Saver JL, Greenstein P, Ronthal M, Mesulam MM. Asymmetric catalepsy after right hemisphere stroke. Mov Disord. 1993; 8(1):69-73. PMID: 8419810.
    View in: PubMed
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