Penzien J - Search Results

1

Evaluation of the 2010 McDonald multiple sclerosis criteria in children with a clinically isolated syndrome.

Kornek B, Schmitl B, Vass K, Zehetmayer S, Pritsch M, Penzien J, Karenfort M, Blaschek A, Seidl R, Prayer D, Rostasy K. Kornek B, et al. Among authors: penzien j. Mult Scler. 2012 Dec;18(12):1768-74. doi: 10.1177/1352458512444661. Epub 2012 Apr 23. Mult Scler. 2012. PMID: 22526931

2

Natalizumab therapy for highly active pediatric multiple sclerosis.

Kornek B, Aboul-Enein F, Rostasy K, Milos RI, Steiner I, Penzien J, Hellwig K, Pitarokoili K, Storm van's Gravesande K, Karenfort M, Blaschek A, Meyer A, Seidl R, Debelic D, Vass K, Prayer D, Kristoferitsch W, Bayas A. Kornek B, et al. Among authors: penzien j. JAMA Neurol. 2013 Apr;70(4):469-75. doi: 10.1001/jamaneurol.2013.923. JAMA Neurol. 2013. PMID: 23420110

3

Accidental natalizumab administration to the third trimester of pregnancy in an adolescent patient with multiple sclerosis.

Bayas A, Penzien J, Hellwig K. Bayas A, et al. Among authors: penzien j. Acta Neurol Scand. 2011 Oct;124(4):290-2. doi: 10.1111/j.1600-0404.2010.01480.x. Epub 2011 Feb 9. Acta Neurol Scand. 2011. PMID: 21943035

4

Accidental natalizumab administration in pregnancy in multiple sclerosis.

Bayas A, Penzien J, Hellwig K. Bayas A, et al. Among authors: penzien j. Acta Neurol Scand. 2012 Jul;126(1):e5-6. doi: 10.1111/j.1600-0404.2011.01636.x. Acta Neurol Scand. 2012. PMID: 22671932 No abstract available.

5

Successful treatment of anti-N-methyl-D-aspartate receptor encephalitis presenting with catatonia.

Schimmel M, Bien CG, Vincent A, Schenk W, Penzien J. Schimmel M, et al. Among authors: penzien j. Arch Dis Child. 2009 Apr;94(4):314-6. doi: 10.1136/adc.2008.149021. Arch Dis Child. 2009. PMID: 19307202

6

Novel truncating and missense mutations of the KCC3 gene associated with Andermann syndrome.

Uyanik G, Elcioglu N, Penzien J, Gross C, Yilmaz Y, Olmez A, Demir E, Wahl D, Scheglmann K, Winner B, Bogdahn U, Topaloglu H, Hehr U, Winkler J. Uyanik G, et al. Among authors: penzien j. Neurology. 2006 Apr 11;66(7):1044-8. doi: 10.1212/01.wnl.0000204181.31175.8b. Neurology. 2006. PMID: 16606917

7

The dynamics of brain concentrations of phenylalanine and its clinical significance in patients with phenylketonuria determined by in vivo 1H magnetic resonance spectroscopy.

Pietz J, Kreis R, Boesch C, Penzien J, Rating D, Herschkowitz N. Pietz J, et al. Among authors: penzien j. Pediatr Res. 1995 Nov;38(5):657-63. doi: 10.1203/00006450-199511000-00005. Pediatr Res. 1995. PMID: 8552430

8

Identification and quantitation of phenylalanine in the brain of patients with phenylketonuria by means of localized in vivo 1H magnetic-resonance spectroscopy.

Kreis R, Pietz J, Penzien J, Herschkowitz N, Boesch C. Kreis R, et al. Among authors: penzien j. J Magn Reson B. 1995 Jun;107(3):242-51. doi: 10.1006/jmrb.1995.1084. J Magn Reson B. 1995. PMID: 7788097

9

[Adult form of metachromatic leukodystrophy with predominantly psychotic manifestations].

Penzien JM, Herschkowitz N, Gieselmann V. Penzien JM, et al. Nervenarzt. 1994 Jan;65(1):73. Nervenarzt. 1994. PMID: 8145880 German. No abstract available.

10

SLC13A5 is the second gene associated with Kohlschütter-Tönz syndrome.

Schossig A, Bloch-Zupan A, Lussi A, Wolf NI, Raskin S, Cohen M, Giuliano F, Jurgens J, Krabichler B, Koolen DA, de Macena Sobreira NL, Maurer E, Muller-Bolla M, Penzien J, Zschocke J, Kapferer-Seebacher I. Schossig A, et al. Among authors: penzien j. J Med Genet. 2017 Jan;54(1):54-62. doi: 10.1136/jmedgenet-2016-103988. Epub 2016 Sep 6. J Med Genet. 2017. PMID: 27600704 Clinical Trial.

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