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Matthias Eckenweiler (1978-)

Kinderarzt

Name	Matthias Eckenweiler
Time	1978- (Date of birth and death)
Place	Hechingen (Geburtsort) Deutschland
Academic degree	Dr. med.
Profession	Kinderarzt (characteristic profession)
Related	Klinik für Neuropädiatrie und Muskelerkrankungen
Further information	Diss. Medizinische Fakultät an der Universität Freiburg im Breisgau Funktionsoberarzt
Record type	Person
GND-Identifier	133032809
Record ID	133032809
Involved in show all Recurrent de novoSPTLC2variant causes childhood-onset amyotrophic lateral sclerosis (ALS) by excess sphingolipid synthesis Long‐term follow‐up of pediatric patients with dyskinetic cerebral palsy and deep brain stimulation CAPRIN1P512L causes aberrant protein aggregation and associates with early-onset ataxia CAPRIN1P512L causes aberrant protein aggregation and associates with early-onset ataxia Quality of life after deep brain stimulation of pediatric patients with dyskinetic cerebral palsy: a prospective, single‐arm, multicenter study with a subsequent randomized double‐blind crossover (STIM-CP) Reversible sensory neuropathy in mitochondrial trifunctional protein deficiency Temporal dynamics of MOG antibodies in children with acquired demyelinating syndrome Temporal dynamics of MOG antibodies in children with acquired demyelinating syndrome Variants in mitochondrial ATP synthase cause variable neurologic phenotypes Measuring the Head Circumference on MRI in Children: an Interrater Study Agammaglobulinemia with normal B-cell numbers in a patient lacking Bob1 Alpers- and MNGIE-like disease with disturbed CSF folate transport and an unusual mode of genetic transmission of POLG mutations: a case report Measuring the head circumference on MRI in children: an interrater study Post‐dural puncture headache - a single‐centre analysis in paediatric patients with and without SMA Scoring algorithm‐based genomic testing in Dystonia: A prospective validation study The spectrum of peripheral neuropathy in disorders of the mitochondrial trifunctional protein Cerebrospinal fluid findings in patients with myelin oligodendrocyte glycoprotein (MOG) antibodies. Part 2: Results from 108 lumbar punctures in 80 pediatric patients Severe Locked-In-Like Guillain–Barré's Syndrome: Dilemmas in Diagnosis and Treatment Thiamine Treatment and Favorable Outcome in an Infant with Biallelic TPK1 Variants Cerebrospinal fluid findings in patients with myelin oligodendrocyte glycoprotein (MOG) antibodies. Part 2: results from 108 lumbar punctures in 80 pediatric patients The intrathecal, polyspecific antiviral immune response in neurosarcoidosis, acute disseminated encephalomyelitis and autoimmuneencephalitis in a tertiary hospital cohort Retrospektive Analyse der Machbarkeit und Effizienz von Granulozytentransfusionen bei Patienten mit schweren Infektionen in der Neutropenie

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Matthias Eckenweiler (1978-)

Recurrent de novoSPTLC2variant causes childhood-onset amyotrophic lateral sclerosis (ALS) by excess sphingolipid synthesis

Long‐term follow‐up of pediatric patients with dyskinetic cerebral palsy and deep brain stimulation

CAPRIN1P512L causes aberrant protein aggregation and associates with early-onset ataxia

CAPRIN1P512L causes aberrant protein aggregation and associates with early-onset ataxia

Quality of life after deep brain stimulation of pediatric patients with dyskinetic cerebral palsy: a prospective, single‐arm, multicenter study with a subsequent randomized double‐blind crossover (STIM-CP)

Reversible sensory neuropathy in mitochondrial trifunctional protein deficiency

Temporal dynamics of MOG antibodies in children with acquired demyelinating syndrome

Temporal dynamics of MOG antibodies in children with acquired demyelinating syndrome

Variants in mitochondrial ATP synthase cause variable neurologic phenotypes

Measuring the Head Circumference on MRI in Children: an Interrater Study

Agammaglobulinemia with normal B-cell numbers in a patient lacking Bob1

Alpers- and MNGIE-like disease with disturbed CSF folate transport and an unusual mode of genetic transmission of POLG mutations: a case report

Measuring the head circumference on MRI in children: an interrater study

Post‐dural puncture headache - a single‐centre analysis in paediatric patients with and without SMA

Scoring algorithm‐based genomic testing in Dystonia: A prospective validation study

The spectrum of peripheral neuropathy in disorders of the mitochondrial trifunctional protein

Cerebrospinal fluid findings in patients with myelin oligodendrocyte glycoprotein (MOG) antibodies. Part 2: Results from 108 lumbar punctures in 80 pediatric patients

Severe Locked-In-Like Guillain–Barré's Syndrome: Dilemmas in Diagnosis and Treatment

Thiamine Treatment and Favorable Outcome in an Infant with Biallelic TPK1 Variants

Cerebrospinal fluid findings in patients with myelin oligodendrocyte glycoprotein (MOG) antibodies. Part 2: results from 108 lumbar punctures in 80 pediatric patients

The intrathecal, polyspecific antiviral immune response in neurosarcoidosis, acute disseminated encephalomyelitis and autoimmuneencephalitis in a tertiary hospital cohort

Retrospektive Analyse der Machbarkeit und Effizienz von Granulozytentransfusionen bei Patienten mit schweren Infektionen in der Neutropenie