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A Randomized Trial of the Effects of Nebulized Albuterol on Pulmonary Edema in Brain‐Dead Organ Donors

American journal of transplantation, 2014-03, Vol.14 (3), p.621-628

2014

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Prospective memory in patients with juvenile myoclonic epilepsy and their healthy siblings

Neurology, 2010-12, Vol.75 (24), p.2161-2167

2010

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The Idiopathic Generalized Epilepsies of Adolescence with Childhood and Juvenile Age of Onset

Epilepsia (Copenhagen), 1997-01, Vol.38 (1), p.4-11

Janz, Dieter

1997

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Maternal Use of Antiepileptic Drugs and the Risk of Major Congenital Malformations: A Joint European Prospective Study of Human Teratogenesis Associated with Maternal Epilepsy

Epilepsia (Copenhagen), 1997-09, Vol.38 (9), p.981-990

1997

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Motor system hyperconnectivity in juvenile myoclonic epilepsy: a cognitive functional magnetic resonance imaging study

Brain (London, England : 1878), 2011-06, Vol.134 (Pt 6), p.1710-1719

2011

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Nonlinear Imputation of PaO2/FIO2 From SpO2/FIO2 Among Mechanically Ventilated Patients in the ICU: A Prospective, Observational Study

Critical care medicine, 2017-08, Vol.45 (8), p.1317-1324

2017

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Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance

Human molecular genetics, 2009-10, Vol.18 (19), p.3626-3631

2009

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Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32

Human molecular genetics, 2012-12, Vol.21 (24), p.5359-5372

2012

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Epilepsy with grand mal on awakening and sleep-waking cycle

Clinical neurophysiology, 2000-09, Vol.111, p.S103-S110

Janz, Dieter

2000

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Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myoclonic epilepsy patients

Neurology, 1991-10, Vol.41 (10), p.1651-1651

1991

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Juvenile myoclonic epilepsy. Epilepsy with impulsive petit mal

Cleveland Clinic journal of medicine, 1989, Vol.56 Suppl Pt 1 (Supplement), p.S23-S-33

Janz, D

1989

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Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6

Neurology, 1997-09, Vol.49 (3), p.842-847

1997

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Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies

Nature genetics, 2003-04, Vol.33 (4), p.527-532

2003

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Neuropathological Findings in Primary Generalized Epilepsy: A Study of Eight Cases

Epilepsia (Copenhagen), 1984-02, Vol.25 (1), p.8-21

1984

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The voltage gated potassium channel KCNQ2 and idiopathic generalized epilepsy

Neuroreport, 1999-04, Vol.10 (6), p.1163-1166

1999

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Do idiopathic generalized epilepsies share a common susceptibility gene?

Neurology, 1992-04, Vol.42 (4 Suppl 5), p.48

1992

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Distinct Molecular Phenotypes of Direct vs Indirect ARDS in Single-Center and Multicenter Studies

Chest, 2015-06, Vol.147 (6), p.1539-1548

2015

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Viktor von Weizsäcker, a founder of psychosomatic medicine

Fortschritte der Neurologie, Psychiatrie, 2001-08, Vol.69 Suppl 1, p.S28-S33

Janz, D

2001

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Sleep Microstructure and EEG Epileptiform Activity in Patients with Juvenile Myoclonic Epilepsy

Epilepsia (Copenhagen), 1992-09, Vol.33 (5), p.799-804

1992

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The Significance of Microdysgenesia in Primary Generalized Epilepsy: An Answer to the Considerations of Lyon and Gastaut

Epilepsia (Copenhagen), 1985-08, Vol.26 (4), p.368-371

1985

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Syndrome-related genetics in generalized epilepsy

Epilepsy research. Supplement, 1991, Vol.4, p.105

1991

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Genome search for susceptibility loci of common idiopathic generalised epilepsies

Human molecular genetics, 2000-06, Vol.9 (10), p.1465-1472

2000

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Length variation of a polyglutamine array in the gene encoding a small-conductance, calcium-activated potassium channel ( hKCa3) and susceptibility to idiopathic generalized epilepsy

Epilepsy research, 1999-02, Vol.33 (2), p.227-233

1999

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No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 5 in families with typical absence seizures

Epilepsy research, 2002-09, Vol.51 (1), p.23-29

2002

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The phenotypic spectrum related to the human epilepsy susceptibility gene "EJM1"

Annals of neurology, 1995-08, Vol.38 (2), p.210-217

1995

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A Randomized Trial of the Effects of Nebulized Albuterol on Pulmonary Edema in Brain‐Dead Organ Donors

Prospective memory in patients with juvenile myoclonic epilepsy and their healthy siblings

The Idiopathic Generalized Epilepsies of Adolescence with Childhood and Juvenile Age of Onset

Maternal Use of Antiepileptic Drugs and the Risk of Major Congenital Malformations: A Joint European Prospective Study of Human Teratogenesis Associated with Maternal Epilepsy

Motor system hyperconnectivity in juvenile myoclonic epilepsy: a cognitive functional magnetic resonance imaging study

Nonlinear Imputation of PaO2/FIO2 From SpO2/FIO2 Among Mechanically Ventilated Patients in the ICU: A Prospective, Observational Study

Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32

Epilepsy with grand mal on awakening and sleep-waking cycle

Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myoclonic epilepsy patients

Juvenile myoclonic epilepsy. Epilepsy with impulsive petit mal

Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6

Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies

Neuropathological Findings in Primary Generalized Epilepsy: A Study of Eight Cases

The voltage gated potassium channel KCNQ2 and idiopathic generalized epilepsy

Do idiopathic generalized epilepsies share a common susceptibility gene?

Distinct Molecular Phenotypes of Direct vs Indirect ARDS in Single-Center and Multicenter Studies

Viktor von Weizsäcker, a founder of psychosomatic medicine

Sleep Microstructure and EEG Epileptiform Activity in Patients with Juvenile Myoclonic Epilepsy

The Significance of Microdysgenesia in Primary Generalized Epilepsy: An Answer to the Considerations of Lyon and Gastaut

Syndrome-related genetics in generalized epilepsy

Genome search for susceptibility loci of common idiopathic generalised epilepsies

Length variation of a polyglutamine array in the gene encoding a small-conductance, calcium-activated potassium channel ( hKCa3) and susceptibility to idiopathic generalized epilepsy

No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 5 in families with typical absence seizures

The phenotypic spectrum related to the human epilepsy susceptibility gene "EJM1"

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