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Antiepileptic drugs and the developing brain

Cellular and molecular life sciences : CMLS, 2006-02, Vol.63 (4), p.399-413

2006

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Acute and long-term proteome changes induced by oxidative stress in the developing brain

Cell death and differentiation, 2006-07, Vol.13 (7), p.1097-1109

2006

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Microglial MyD88 signaling regulates acute neuronal toxicity of LPS-stimulated microglia in vitro

Brain, behavior, and immunity, 2010-07, Vol.24 (5), p.776-783

2010

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The Triple A Syndrome Is Due to Mutations in ALADIN, a Novel Member of the Nuclear Pore Complex

Endocrine research, 2004-01, Vol.30 (4), p.891-899

2004

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Mutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like disease

American journal of human genetics, 2004-08, Vol.75 (2), p.251-260

2004

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Neuronal death and oxidative stress in the developing brain

Antioxidants & redox signaling, 2011-04, Vol.14 (8), p.1535-1550

2011

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Facing the genetic heterogeneity in neuromuscular disorders: Linkage analysis as an economic diagnostic approach towards the molecular diagnosis

Neuromuscular disorders : NMD, 2006-01, Vol.16 (1), p.4-13

2006

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Missense mutations of ACTA1 cause dominant congenital myopathy with cores

Journal of medical genetics, 2004-11, Vol.41 (11), p.842-848

2004

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Centrosomes, Cilia, and Microcephaly

Neuropediatrics, 2017, Vol.48 (S 01), p.S1-S45

Kaindl, A.

2017

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Treating Neonates with Levetiracetam: a survey among German University Hospitals

Klinische Padiatrie, 2011-12, Vol.223 (7), p.450

2011

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NEW INSIGHTS INTO THE MOLECULAR BASIS OF THE TRIPLE A SYNDROME

Endocrine research, 2002-01, Vol.28 (4), p.733-739

2002

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Novel RYR1 missense mutation causes core rod myopathy

European journal of neurology, 2008-04, Vol.15 (4), p.e31-e32

2008

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In utero development of symmetric thalamic and brainstem necrosis in a preterm hydropic stillborn

Clinical neuropathology, 2010-11, Vol.29 (6), p.365-371

2010

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Acute Ascending Motoric Paraplegia Following Intrathecal Chemotherapy for Treatment of Acute Lymphoblastic Leukemia in Children: Case Reports and Review of the Literature

Klinische Pädiatrie, 2006-11, Vol.218 (6), p.350-354

2006

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Lacosamide Lowers Valproate and Levetiracetam Levels

Neuropediatrics, 2017, Vol.48 (S 01), p.S1-S45

2017

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Pathological Fractures in Patients with Myelomeningocele

Neuropediatrics, 2017, Vol.48 (S 01), p.S1-S45

2017

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Distal spinal-muscular atrophy 1 (DSMA1 or SMARD1)

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2008-10, Vol.15 (10), p.1568-1572

2008

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Congenital Muscular Dystrophy-Dystroglycanopathy (MDDGA1) in a Consanguineous Family with Compound Heterozygous Mutations of the POMT1 Gene and Variable Clinical Severity

Neuropediatrics, 2016, Vol.47 (S 01)

2016

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A Novel Phenotype: Microcephaly, Intellectual Disability, and Mid-hindbrain Defect

Neuropediatrics, 2014, Vol.45 (S 01)

2014

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Sulthiame but not levetiracetam exerts neurotoxic effect in the developing rat brain

Experimental neurology, 2005-06, Vol.193 (2), p.497-503

2005

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Immunodeficiency, Centromeric Instability, Facial Anomalies Syndrome Type 2 (ICF2): Combined Immunodeficiency, Autoimmune Phenomena, and Intellectual Disability

Neuropediatrics, 2014, Vol.45 (S 01)

2014

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Corrigendum to “Microglial MyD88 signaling regulates acute neuronal toxicity of LPS-stimulated microglia in vitro” [Brain Behav. Immun. 24 (2010) 776–783]

Brain, behavior, and immunity, 2011-01, Vol.25 (1), p.175-175

2011

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Abnormal Distribution of Calcium-Handling Proteins: A Novel Distinctive Marker in Core Myopathies

Journal of neuropathology and experimental neurology, 2007-01, Vol.66 (1), p.57-65

2007

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Protection with estradiol in developmental models of apoptotic neurodegeneration

Annals of neurology, 2005-08, Vol.58 (2), p.266-276

2005

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Phenotype Variability of Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease IMNEPD

Neuropediatrics, 2016, Vol.47 (S 01)

2016

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Antiepileptic drugs and the developing brain

Acute and long-term proteome changes induced by oxidative stress in the developing brain

Microglial MyD88 signaling regulates acute neuronal toxicity of LPS-stimulated microglia in vitro

The Triple A Syndrome Is Due to Mutations in ALADIN, a Novel Member of the Nuclear Pore Complex

Mutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like disease

Neuronal death and oxidative stress in the developing brain

Facing the genetic heterogeneity in neuromuscular disorders: Linkage analysis as an economic diagnostic approach towards the molecular diagnosis

Missense mutations of ACTA1 cause dominant congenital myopathy with cores

Centrosomes, Cilia, and Microcephaly

Treating Neonates with Levetiracetam: a survey among German University Hospitals

NEW INSIGHTS INTO THE MOLECULAR BASIS OF THE TRIPLE A SYNDROME

Novel RYR1 missense mutation causes core rod myopathy

In utero development of symmetric thalamic and brainstem necrosis in a preterm hydropic stillborn

Acute Ascending Motoric Paraplegia Following Intrathecal Chemotherapy for Treatment of Acute Lymphoblastic Leukemia in Children: Case Reports and Review of the Literature

Lacosamide Lowers Valproate and Levetiracetam Levels

Pathological Fractures in Patients with Myelomeningocele

Distal spinal-muscular atrophy 1 (DSMA1 or SMARD1)

Congenital Muscular Dystrophy-Dystroglycanopathy (MDDGA1) in a Consanguineous Family with Compound Heterozygous Mutations of the POMT1 Gene and Variable Clinical Severity

A Novel Phenotype: Microcephaly, Intellectual Disability, and Mid-hindbrain Defect

Sulthiame but not levetiracetam exerts neurotoxic effect in the developing rat brain

Immunodeficiency, Centromeric Instability, Facial Anomalies Syndrome Type 2 (ICF2): Combined Immunodeficiency, Autoimmune Phenomena, and Intellectual Disability

Corrigendum to “Microglial MyD88 signaling regulates acute neuronal toxicity of LPS-stimulated microglia in vitro” [Brain Behav. Immun. 24 (2010) 776–783]

Abnormal Distribution of Calcium-Handling Proteins: A Novel Distinctive Marker in Core Myopathies

Protection with estradiol in developmental models of apoptotic neurodegeneration

Phenotype Variability of Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease IMNEPD

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