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Gerhard Kurlemann

Arzt

Name	Gerhard Kurlemann
Place	Deutschland
Academic degree	Univ.-Prof. Dr. med.
Profession	Arzt
Variant	Gerd Kurlemann
Related	Universitätsklinikum Münster St.-Bonifatius-Hospital (Lingen (Ems))
Further information	Professor am Zentrum für Kinderheilkunde, Abteilung für Neuropädiatrie, Universitätsklinikum Münster; seit 2018 Kinderklinik Lingen
Record type	Person
GND-Identifier	109380746
Record ID	109380746
Involved in show all Giant axonal neuropathy (GAN): cross-sectional data on phenotypes, genotypes, and proteomic signature from a German cohort Vorurteile, Wissen und Einstellungen zum Krankheitsbild Epilepsie von Betroffenen und ihren Angehörigen Characterization of the Epileptogenic Phenotype and Response to Antiseizure Medications in Lissencephaly Patients A multicenter, matched case–control analysis comparing burden of illness among patients with tuberous sclerosis complex related epilepsy, generalized idiopathic epilepsy, and focal epilepsy in Germany Fenfluramine in clinical practice: new therapy option for Dravet and Lennox–Gastaut syndromes Clinical characteristics and quality of life with Dravet syndrome: results of the German cohort of the Dravet syndrome caregiver survey (DISCUSS) = Klinische Charakteristika und Lebensqualität beim Dravet-Syndrom: Ergebnisse der deutschen Kohorte des „Dravet syndrome caregiver survey“ (DISCUSS) Critical incidents, nocturnal supervision, and caregiver knowledge on SUDEP in patients with Dravet syndrome: a prospective multicenter study in Germany Eine Befragung von Kindern und Jugendlichen mit Epilepsie oder Asthma bronchiale über Einfluss und Auswirkungen der chronischen Erkrankung auf Geschwisterkinder und die Geschwisterbeziehung. Sleep quality, anxiety, symptoms of depression, and caregiver burden among those caring for patients with Dravet syndrome: a prospective multicenter study in Germany Exploring the relationships between composite scores of disease severity, seizure-freedom and quality of life in Dravet syndrome L-Serine Treatment is Associated with Improvements in Behavior, EEG, and Seizure Frequency in Individuals with GRIN-Related Disorders Due to Null Variants Treatment of Infantile Spasm Syndrome: Update from the Interdisciplinary Guideline Committee Coordinated by the German-Speaking Society of Neuropediatrics Klinische Charakteristika und Lebensqualität beim Dravet-Syndrom: Ergebnisse der deutschen Kohorte des „Dravet syndrome caregiver survey“ (DISCUSS) = Clinical characteristics and quality of life with Dravet syndrome: results of the German cohort of the Dravet syndrome caregiver survey (DISCUSS) L-serine treatment is associated with improvements in behavior, EEG, and seizure frequency in individuals with GRIN-related disorders due to null variants Treatment of infantile spasm syndrome: update from the interdisciplinary guideline committee coordinated by the German-speaking Society of Neuropediatrics Efficacy, Retention and Tolerability of Everolimus in Patients with Tuberous Sclerosis Complex: A Survey-Based Study on Patients’ Perspectives Quality of life and its predictors in adults with tuberous sclerosis complex (TSC): a multicentre cohort study from Germany Direct and indirect costs and cost-driving factors of Tuberous sclerosis complex in children, adolescents, and caregivers: a multicenter cohort study Direct and indirect costs and cost-driving factors in adults with tuberous sclerosis complex: a multicenter cohort study and a review of the literature Direct and indirect costs and cost-driving factors in adults with tuberous sclerosis complex: a multicenter cohort study and a review of the literature Efficacy, tolerability, and retention of fenfluramine for the treatment of seizures in patients with Dravet syndrome: compassionate use program in Germany Efficacy, tolerability, and retention of fenfluramine for the treatment of seizures in patients with Dravet syndrome: compassionate use program in Germany Efficacy, tolerability, and retention of fenfluramine for the treatment of seizures in patients with Dravet syndrome: Compassionate use program in Germany Efficacy, tolerability, and retention of fenfluramine for the treatment of seizures in patients with Dravet syndrome: Compassionate use program in Germany Long-term efficacy, tolerability, and retention of brivaracetam in epilepsy treatment: a longitudinal multicenter study with up to 5 years of follow-up Long-term efficacy, tolerability, and retention of brivaracetam in epilepsy treatment: a longitudinal multicenter study with up to 5 years of follow-up Übungsbuch EEG bei Kindern und Jugendlichen : Atlas mit 370 Beispielen Klinische Charakteristika, Ressourcenverbrauch, Lebensqualität und Versorgungssituation beim Dravet-Syndrom in Deutschland Burden-of-illness and cost-driving factors in Dravet syndrome patients and carers : a prospective, multicenter study from Germany Aufgaben und Struktur moderner Epilepsiezentren in Deutschland Efficacy, retention, and tolerability of Brivaracetam in patients with epileptic encephalopathies : a multicenter cohort study from Germany Treatment of Infantile Spasms: Report of the Interdisciplinary Guideline Committee Coordinated by the German-Speaking Society for Neuropediatrics Effectiveness and Tolerability of Perampanel in Children and Adolescents with Refractory Epilepsies: First Experiences Epilepsie im Kindesalter: Wann kann die antiepileptische Therapie abgesetzt werden? : Eine Meinungsäußerung des Königsteiner Arbeitskreises Leichtes Schädelhirntrauma im Kindesalter Neurokutane Syndrome und Epilepsie : Neurofibromatose, tuberöse Sklerose, andere Phakomatosen Epilepsie und Hormone Entwicklung und neurologische Störungen nach kontrollierter Langzeitbeatmung in der Neugeborenenperiode : Nachuntersuchung an 21 überlebenden Kindern

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Katalog der Deutschen Nationalbibliothek

Gerhard Kurlemann

Giant axonal neuropathy (GAN): cross-sectional data on phenotypes, genotypes, and proteomic signature from a German cohort

Vorurteile, Wissen und Einstellungen zum Krankheitsbild Epilepsie von Betroffenen und ihren Angehörigen

Characterization of the Epileptogenic Phenotype and Response to Antiseizure Medications in Lissencephaly Patients

A multicenter, matched case–control analysis comparing burden of illness among patients with tuberous sclerosis complex related epilepsy, generalized idiopathic epilepsy, and focal epilepsy in Germany

Fenfluramine in clinical practice: new therapy option for Dravet and Lennox–Gastaut syndromes

Critical incidents, nocturnal supervision, and caregiver knowledge on SUDEP in patients with Dravet syndrome: a prospective multicenter study in Germany

Eine Befragung von Kindern und Jugendlichen mit Epilepsie oder Asthma bronchiale über Einfluss und Auswirkungen der chronischen Erkrankung auf Geschwisterkinder und die Geschwisterbeziehung.

Sleep quality, anxiety, symptoms of depression, and caregiver burden among those caring for patients with Dravet syndrome: a prospective multicenter study in Germany

Exploring the relationships between composite scores of disease severity, seizure-freedom and quality of life in Dravet syndrome

L-Serine Treatment is Associated with Improvements in Behavior, EEG, and Seizure Frequency in Individuals with GRIN-Related Disorders Due to Null Variants

Treatment of Infantile Spasm Syndrome: Update from the Interdisciplinary Guideline Committee Coordinated by the German-Speaking Society of Neuropediatrics

L-serine treatment is associated with improvements in behavior, EEG, and seizure frequency in individuals with GRIN-related disorders due to null variants

Treatment of infantile spasm syndrome: update from the interdisciplinary guideline committee coordinated by the German-speaking Society of Neuropediatrics

Efficacy, Retention and Tolerability of Everolimus in Patients with Tuberous Sclerosis Complex: A Survey-Based Study on Patients’ Perspectives

Quality of life and its predictors in adults with tuberous sclerosis complex (TSC): a multicentre cohort study from Germany

Direct and indirect costs and cost-driving factors of Tuberous sclerosis complex in children, adolescents, and caregivers: a multicenter cohort study

Direct and indirect costs and cost-driving factors in adults with tuberous sclerosis complex: a multicenter cohort study and a review of the literature

Direct and indirect costs and cost-driving factors in adults with tuberous sclerosis complex: a multicenter cohort study and a review of the literature

Efficacy, tolerability, and retention of fenfluramine for the treatment of seizures in patients with Dravet syndrome: compassionate use program in Germany

Efficacy, tolerability, and retention of fenfluramine for the treatment of seizures in patients with Dravet syndrome: compassionate use program in Germany

Efficacy, tolerability, and retention of fenfluramine for the treatment of seizures in patients with Dravet syndrome: Compassionate use program in Germany

Efficacy, tolerability, and retention of fenfluramine for the treatment of seizures in patients with Dravet syndrome: Compassionate use program in Germany

Long-term efficacy, tolerability, and retention of brivaracetam in epilepsy treatment: a longitudinal multicenter study with up to 5 years of follow-up

Long-term efficacy, tolerability, and retention of brivaracetam in epilepsy treatment: a longitudinal multicenter study with up to 5 years of follow-up

Übungsbuch EEG bei Kindern und Jugendlichen : Atlas mit 370 Beispielen

Klinische Charakteristika, Ressourcenverbrauch, Lebensqualität und Versorgungssituation beim Dravet-Syndrom in Deutschland

Burden-of-illness and cost-driving factors in Dravet syndrome patients and carers : a prospective, multicenter study from Germany

Aufgaben und Struktur moderner Epilepsiezentren in Deutschland

Efficacy, retention, and tolerability of Brivaracetam in patients with epileptic encephalopathies : a multicenter cohort study from Germany

Treatment of Infantile Spasms: Report of the Interdisciplinary Guideline Committee Coordinated by the German-Speaking Society for Neuropediatrics

Effectiveness and Tolerability of Perampanel in Children and Adolescents with Refractory Epilepsies: First Experiences

Epilepsie im Kindesalter: Wann kann die antiepileptische Therapie abgesetzt werden? : Eine Meinungsäußerung des Königsteiner Arbeitskreises

Leichtes Schädelhirntrauma im Kindesalter

Neurokutane Syndrome und Epilepsie : Neurofibromatose, tuberöse Sklerose, andere Phakomatosen

Epilepsie und Hormone

Entwicklung und neurologische Störungen nach kontrollierter Langzeitbeatmung in der Neugeborenenperiode : Nachuntersuchung an 21 überlebenden Kindern