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

Archives of disease in childhood, 2009-04, Vol.94 (4), p.314-316

2009

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

Acta neurologica Scandinavica, 2011-10, Vol.124 (4), p.290-292

2011

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Effects of cholesterol and simvastatin treatment in patients with Smith-Lemli-Opitz syndrome (SLOS)

Journal of inherited metabolic disease, 2007-06, Vol.30 (3), p.375-387

2007

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Mutations in the Sepiapterin Reductase Gene Cause a Novel Tetrahydrobiopterin-Dependent Monoamine-Neurotransmitter Deficiency without Hyperphenylalaninemia

American journal of human genetics, 2001-08, Vol.69 (2), p.269-277

2001

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Accidental natalizumab administration in pregnancy in multiple sclerosis

Acta neurologica Scandinavica, 2012-07, Vol.126 (1), p.e5-e6

2012

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

Neurology, 2006-04, Vol.66 (7), p.1044-1048

2006

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Seismically induced racking of tunnel linings

Earthquake engineering & structural dynamics, 2000-05, Vol.29 (5), p.683-691

Penzien, Joseph

2000

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Pediatric and adult multiple sclerosis — /INS;Comparison of magnetic resonance imaging characteristics at disease onset

Journal of the neurological sciences, 2013-10, Vol.333, p.e385-e386

2013

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The role of protons in hydroamination reactions involving homogeneous and heterogeneous catalysts

Journal of molecular catalysis. A, Chemical, 2002-05, Vol.182, p.489-498

2002

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Congenital disorder of glycosylation IId (CDG-IId) -- a new entity: clinical presentation with Dandy-Walker malformation and myopathy

Neuropediatrics, 2002-02, Vol.33 (1), p.27-32

2002

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Molecular and functional characterisation of mild MCAD deficiency

Human genetics, 2001-05, Vol.108 (5), p.404-408

2001

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Variant of dihydropteridine reductase deficiency without hyperphenylalaninaemia: Effect of oral phenylalanine loading

Journal of inherited metabolic disease, 1999-05, Vol.22 (3), p.216-220

1999

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Improvement of SSPE after carbamazepine: natural course or therapeutic effect?

Neuropediatrics, 2010, Vol.41 (2)

2010

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Generation and Characterization of Well-Defined Zn2+ Lewis Acid Sites in Ion Exchanged Zeolite BEA

The journal of physical chemistry. B, 2004-04, Vol.108 (13), p.4116-4126

2004

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Severe Hepatotoxicity During Valproate Therapy: An Update and Report of Eight New Fatalities

Epilepsia (Copenhagen), 1994-09, Vol.35 (5), p.1005-1015

1994

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Cranial MRI changes may precede symptoms in Hallervorden-Spatz syndrome

Pediatric neurology, 2001-08, Vol.25 (2), p.166-169

2001

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Multiple-station ground motion processing and simulation based on smart-1 array data

Nuclear engineering and design, 1989-02, Vol.111 (3), p.293-310

1989

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Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders

European journal of human genetics : EJHG, 2013-10, Vol.21 (10), p.1074-1078

2013

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

Acta neurologica Scandinavica, 2011-10, Vol.124 (4), p.290-292

2011

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Valproate (VPA) Metabolites in Various Clinical Conditions of Probable VPA‐Associated Hepatotoxicity

Epilepsia (Copenhagen), 1993-03, Vol.34 (2), p.332-346

1993

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Compound heterozygosity for metachromatic leukodystrophy and arylsulfatase A pseudodeficiency alleles is not associated with progressive neurological disease

American journal of human genetics, 1993-03, Vol.52 (3), p.557-564

1993

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Evaluation of building separation distance required to prevent pounding during strong earthquakes

Earthquake engineering & structural dynamics, 1997-08, Vol.26 (8), p.849-858

Penzien, Joseph

1997

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Special Issue on Earthquake Engineering for Transportation Structures

Earthquake engineering & structural dynamics, 2005-04, Vol.34 (4-5), p.325-326

Penzien, Joseph

2005

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Benign epilepsy with centrotemporal spikes: Correlating spike frequency and neuropsychology

Acta neurologica Scandinavica, 2018-12, Vol.138 (6), p.475-481

2018

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

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

Effects of cholesterol and simvastatin treatment in patients with Smith-Lemli-Opitz syndrome (SLOS)

Mutations in the Sepiapterin Reductase Gene Cause a Novel Tetrahydrobiopterin-Dependent Monoamine-Neurotransmitter Deficiency without Hyperphenylalaninemia

Accidental natalizumab administration in pregnancy in multiple sclerosis

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

Seismically induced racking of tunnel linings

Pediatric and adult multiple sclerosis — /INS;Comparison of magnetic resonance imaging characteristics at disease onset

The role of protons in hydroamination reactions involving homogeneous and heterogeneous catalysts

Congenital disorder of glycosylation IId (CDG-IId) -- a new entity: clinical presentation with Dandy-Walker malformation and myopathy

Molecular and functional characterisation of mild MCAD deficiency

Variant of dihydropteridine reductase deficiency without hyperphenylalaninaemia: Effect of oral phenylalanine loading

Improvement of SSPE after carbamazepine: natural course or therapeutic effect?

Generation and Characterization of Well-Defined Zn2+ Lewis Acid Sites in Ion Exchanged Zeolite BEA

Severe Hepatotoxicity During Valproate Therapy: An Update and Report of Eight New Fatalities

Cranial MRI changes may precede symptoms in Hallervorden-Spatz syndrome

Multiple-station ground motion processing and simulation based on smart-1 array data

Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders

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

Valproate (VPA) Metabolites in Various Clinical Conditions of Probable VPA‐Associated Hepatotoxicity

Compound heterozygosity for metachromatic leukodystrophy and arylsulfatase A pseudodeficiency alleles is not associated with progressive neurological disease

Novel TMEM67 mutations and genotype-phenotype correlates in meckelin-related ciliopathies

Evaluation of building separation distance required to prevent pounding during strong earthquakes

Special Issue on Earthquake Engineering for Transportation Structures

Benign epilepsy with centrotemporal spikes: Correlating spike frequency and neuropsychology

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