Harvard Catalyst Profiles

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Franziska Hoche, M.D.

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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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PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
  1. Schmahmann JD, Vangel MG, Hoche F, Guell X, Sherman JC. Reply: Reference values for the Cerebellar Cognitive Affective Syndrome Scale: age and education matter. Brain. 2021 03 03; 144(2):e21. PMID: 33313688.
    Citations:    Fields:    Translation:Humans
  2. Hoche F, Daly MP, Chutake YK, Valera E, Sherman JC, Schmahmann JD. The Cerebellar Cognitive Affective Syndrome in Ataxia-Telangiectasia. Cerebellum. 2019 Apr; 18(2):225-244. PMID: 30338439.
    Citations: 3     Fields:    Translation:Humans
  3. Hoche F, Guell X, Vangel MG, Sherman JC, Schmahmann JD. The cerebellar cognitive affective/Schmahmann syndrome scale. Brain. 2018 01 01; 141(1):248-270. PMID: 29206893.
    Citations: 56     Fields:    Translation:Humans
  4. Hoche F, Guell X, Sherman JC, Vangel MG, Schmahmann JD. Cerebellar Contribution to Social Cognition. Cerebellum. 2016 12; 15(6):732-743. PMID: 26585120.
    Citations: 42     Fields:    Translation:Humans
  5. Guell X, Hoche F, Schmahmann JD. Metalinguistic deficits in patients with cerebellar dysfunction: empirical support for the dysmetria of thought theory. Cerebellum. 2015 Feb; 14(1):50-8. PMID: 25503825.
    Citations: 19     Fields:    Translation:Humans
  6. Hoche F, Seidel K, Barbosa-Sicard E, Heidegger T, Kang JS, Koenig R, Kieslich M. Novel N-terminal truncating CLCN1 mutation in severe Becker disease. Muscle Nerve. 2014 Nov; 50(5):866-7. PMID: 24920213.
    Citations: 3     Fields:    Translation:Humans
  7. Voss S, Pietzner J, Hoche F, Taylor AM, Last JI, Schubert R, Zielen S. Growth retardation and growth hormone deficiency in patients with Ataxia telangiectasia. Growth Factors. 2014 Jun; 32(3-4):123-9. PMID: 25060036.
    Citations: 11     Fields:    Translation:Humans
  8. Hoche F, Frankenberg E, Rambow J, Theis M, Harding JA, Qirshi M, Seidel K, Barbosa-Sicard E, Porto L, Schmahmann JD, Kieslich M. Cognitive phenotype in ataxia-telangiectasia. Pediatr Neurol. 2014 Sep; 51(3):297-310. PMID: 25037873.
    Citations: 17     Fields:    Translation:Humans
  9. Rüb U, Farrag K, Seidel K, Brunt ER, Heinsen H, Bürk K, Melegh B, von Gall C, Auburger G, Bohl J, Korf HW, Hoche F, den Dunnen W. Involvement of the cholinergic basal forebrain nuclei in spinocerebellar ataxia type 2 (SCA2). Neuropathol Appl Neurobiol. 2013 Oct; 39(6):634-43. PMID: 23363055.
    Citations: 6     Fields:    Translation:HumansCells
  10. Hoche F, Qirshi M, Heidegger T, Kang JS, Koenig R, Kieslich M. Description of a novel c.374 G>A mutation in Becker disease. Muscle Nerve. 2013 Apr; 47(4):616-7. PMID: 23456831.
    Citations:    Fields:    Translation:Humans
  11. Rüb U, Hoche F, Brunt ER, Heinsen H, Seidel K, Del Turco D, Paulson HL, Bohl J, von Gall C, Vonsattel JP, Korf HW, den Dunnen WF. Degeneration of the cerebellum in Huntington's disease (HD): possible relevance for the clinical picture and potential gateway to pathological mechanisms of the disease process. Brain Pathol. 2013 Mar; 23(2):165-77. PMID: 22925167.
    Citations: 37     Fields:    Translation:HumansCells
  12. Hoche F, Seidel K, Theis M, Vlaho S, Schubert R, Zielen S, Kieslich M. Neurodegeneration in ataxia telangiectasia: what is new? What is evident? Neuropediatrics. 2012 Jun; 43(3):119-29. PMID: 22614068.
    Citations: 19     Fields:    Translation:HumansCells
  13. Hoche F, Balikó L, den Dunnen W, Steinecker K, Bartos L, Sáfrány E, Auburger G, Deller T, Korf HW, Klockgether T, Rüb U, Melegh B. Spinocerebellar ataxia type 2 (SCA2): identification of early brain degeneration in one monozygous twin in the initial disease stage. Cerebellum. 2011 Jun; 10(2):245-53. PMID: 21128038.
    Citations: 11     Fields:    Translation:HumansCells
  14. Hoche F, Pfeifenbring S, Vlaho S, Qirshi M, Theis M, Schneider W, Porto L, Müller K, Kieslich M. Rare brain biopsy findings in a first ADEM-like event of pediatric MS: histopathologic, neuroradiologic and clinical features. J Neural Transm (Vienna). 2011 Sep; 118(9):1311-7. PMID: 21547392.
    Citations: 3     Fields:    Translation:HumansCells
  15. Kieslich M, Hoche F, Reichenbach J, Weidauer S, Porto L, Vlaho S, Schubert R, Zielen S. Extracerebellar MRI-lesions in ataxia telangiectasia go along with deficiency of the GH/IGF-1 axis, markedly reduced body weight, high ataxia scores and advanced age. Cerebellum. 2010 Jun; 9(2):190-7. PMID: 19898915.
    Citations: 11     Fields:    Translation:Humans
  16. Hoche F, Seidel K, Brunt ER, Auburger G, Schöls L, Bürk K, de Vos RA, den Dunnen W, Bechmann I, Egensperger R, Van Broeckhoven C, Gierga K, Deller T, Rüb U. Involvement of the auditory brainstem system in spinocerebellar ataxia type 2 (SCA2), type 3 (SCA3) and type 7 (SCA7). Neuropathol Appl Neurobiol. 2008 Oct; 34(5):479-91. PMID: 18221259.
    Citations: 8     Fields:    Translation:Humans
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.