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Angela M. Kaindl (1975-)

Kinderärztin

Name	Angela M. Kaindl
Zeit	1975- (Lebensdaten)
Ort	Deutschland
Akademischer Grad bzw. Titel	Prof. Dr. med.
Beruf	Kinderärztin (charakteristischer Beruf)
Beziehung	Charité - Universitätsmedizin Berlin. Sozialpädiatrisches Zentrum (SPZ) der Charité (Leiterin)
Weitere Angaben	Diss. Fachbereich Humanmedizin
Datensatztyp	Person
GND-Nummer	123725658
Datensatz-ID	123725658
Beteiligt an alle anzeigen Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings Membrane potential states gate synaptic consolidation in human neocortical tissue Applications of OPM-MEG for translational neuroscience: a perspective Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings Neural correlates and reinstatement of recent and remote memory: A comparison between children and young adults Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings Short- and long-delay consolidation of memory accessibility and precision across childhood and young adulthood Pediatric de novo movement disorders and ataxia in the context of SARS-CoV-2 Family Burden and Epilepsy Surgery in Children with Drug-Resistant Epilepsy Epilepsy surgery in early infancy : : a retrospective, multicenter study Neural correlates and reinstatement of recent and remote memory: A comparison between children and young adults Neuropädiatrie Neuropädiatrie Real‐world data on cannabidiol treatment of various epilepsy subtypes: a retrospective, multicenter study Retrospective pediatric cohort study validates NEOS score and demonstrates applicability in children with anti-NMDAR encephalitis PTRH2 is Necessary for Purkinje Cell Differentiation and Survival and its Loss Recapitulates Progressive Cerebellar Atrophy and Ataxia Seen in IMNEPD Patients Handlungsempfehlungen nach der Leitlinie Klassifikation und Diagnostik der Mikrozephalie Atypical NMDA receptor expression in a diffuse astrocytoma, MYB- or MYBL1-altered as a trigger for autoimmune encephalitis Improvement of bladder function after bladder augmentation surgery: a report of 26 years of clinical experience Distinct multivariate structural brain profiles are related to variations in short- and long-delay memory consolidation across children and young adults Distinct multivariate structural brain profiles are related to variations in short- and long-delay memory consolidation across children and young adults Spinale Muskelatrophie bei Kindern und Jugendlichen Motor and functional outcome of selective dorsal rhizotomy in children with spastic diplegia at 12 and 24 months of follow-up Assessment of myelination in infants and young children by T1 relaxation time measurements using the magnetization-prepared 2 rapid acquisition gradient echoes sequence Evaluation of Metabolic Effects of Nusinersen in Patients with Spinal Muscular Atrophy Lumbar Puncture Opening Pressure in Patients with Spinal Muscular Atrophy From learning to remembering: how memory consolidation differs in term and preterm born children from young adults The clinical-phenotype continuum in DYNC1H1-related disorders—genomic profiling and proposal for a novel classification Early Onset, Long Illness Duration, Epilepsy Type, and Polypharmacy Have an Adverse Effect on Psychosocial Outcome in Children with Epilepsy Just Expect It: Compound Heterozygous Variants of POMT1 in a Consanguineous Family—The Role of Next Generation Sequencing in Neuromuscular Disorders Structural brain anomalies in patients with FOX1 syndrome and in Foxg1+/− mice Lacosamide Lowers Valproate and Levetiracetam Levels Phenotype variability of infantile-onset multisystem neurologic, endocrine, and pancreatic disease IMNEPD Neuropädiatrische Differenzialdiagnostik der Mikrozephalie im Kindesalter Neuropädiatrische Differenzialdiagnostik der Mikrozephalie im Kindesalter Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation Combined immunodeficiency develops with age in Immunodeficiency-centromeric instability-facial anomalies syndrome 2 (ICF2) Combined immunodeficiency develops with age in Immunodeficiency-centromeric instability-facial anomalies syndrome 2 (ICF2) Large homozygous RAB3GAP1 gene microdeletion causes Warburg Micro Syndrome 1 Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation Proteome changes associated with developmental defects following perinatally acquired brain damage Phenotype of five patients with dopa-responsive dystonia and mutations in GCH1 Genetic analysis of mouse proteome in two dimensional protein patterns of heart and liver

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Katalog der Deutschen Nationalbibliothek

Angela M. Kaindl (1975-)

Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings

Membrane potential states gate synaptic consolidation in human neocortical tissue

Applications of OPM-MEG for translational neuroscience: a perspective

Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings

Neural correlates and reinstatement of recent and remote memory: A comparison between children and young adults

Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings

Short- and long-delay consolidation of memory accessibility and precision across childhood and young adulthood

Pediatric de novo movement disorders and ataxia in the context of SARS-CoV-2

Family Burden and Epilepsy Surgery in Children with Drug-Resistant Epilepsy

Epilepsy surgery in early infancy : : a retrospective, multicenter study

Neural correlates and reinstatement of recent and remote memory: A comparison between children and young adults

Neuropädiatrie

Neuropädiatrie

Real‐world data on cannabidiol treatment of various epilepsy subtypes: a retrospective, multicenter study

Retrospective pediatric cohort study validates NEOS score and demonstrates applicability in children with anti-NMDAR encephalitis

PTRH2 is Necessary for Purkinje Cell Differentiation and Survival and its Loss Recapitulates Progressive Cerebellar Atrophy and Ataxia Seen in IMNEPD Patients

Handlungsempfehlungen nach der Leitlinie Klassifikation und Diagnostik der Mikrozephalie

Atypical NMDA receptor expression in a diffuse astrocytoma, MYB- or MYBL1-altered as a trigger for autoimmune encephalitis

Improvement of bladder function after bladder augmentation surgery: a report of 26 years of clinical experience

Distinct multivariate structural brain profiles are related to variations in short- and long-delay memory consolidation across children and young adults

Distinct multivariate structural brain profiles are related to variations in short- and long-delay memory consolidation across children and young adults

Spinale Muskelatrophie bei Kindern und Jugendlichen

Motor and functional outcome of selective dorsal rhizotomy in children with spastic diplegia at 12 and 24 months of follow-up

Assessment of myelination in infants and young children by T1 relaxation time measurements using the magnetization-prepared 2 rapid acquisition gradient echoes sequence

Evaluation of Metabolic Effects of Nusinersen in Patients with Spinal Muscular Atrophy

Lumbar Puncture Opening Pressure in Patients with Spinal Muscular Atrophy

From learning to remembering: how memory consolidation differs in term and preterm born children from young adults

The clinical-phenotype continuum in DYNC1H1-related disorders—genomic profiling and proposal for a novel classification

Early Onset, Long Illness Duration, Epilepsy Type, and Polypharmacy Have an Adverse Effect on Psychosocial Outcome in Children with Epilepsy

Just Expect It: Compound Heterozygous Variants of POMT1 in a Consanguineous Family—The Role of Next Generation Sequencing in Neuromuscular Disorders

Structural brain anomalies in patients with FOX1 syndrome and in Foxg1+/− mice

Lacosamide Lowers Valproate and Levetiracetam Levels

Phenotype variability of infantile-onset multisystem neurologic, endocrine, and pancreatic disease IMNEPD

Neuropädiatrische Differenzialdiagnostik der Mikrozephalie im Kindesalter

Neuropädiatrische Differenzialdiagnostik der Mikrozephalie im Kindesalter

Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation

Combined immunodeficiency develops with age in Immunodeficiency-centromeric instability-facial anomalies syndrome 2 (ICF2)

Combined immunodeficiency develops with age in Immunodeficiency-centromeric instability-facial anomalies syndrome 2 (ICF2)

Large homozygous RAB3GAP1 gene microdeletion causes Warburg Micro Syndrome 1

Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation

Proteome changes associated with developmental defects following perinatally acquired brain damage

Phenotype of five patients with dopa-responsive dystonia and mutations in GCH1

Genetic analysis of mouse proteome in two dimensional protein patterns of heart and liver