X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (3) 3
bects (2) 2
behavior (2) 2
child (2) 2
child abuse (2) 2
clinical neurology (2) 2
epilepsy (2) 2
epilepsy, rolandic - psychology (2) 2
female (2) 2
humans (2) 2
intelligence tests (2) 2
male (2) 2
neurology (2) 2
neuropsychological tests (2) 2
pediatrics (2) 2
sulthiame (2) 2
abusive head trauma (1) 1
academic achievement (1) 1
activities of daily living (1) 1
age (1) 1
aging (1) 1
alzheimers disease (1) 1
analysis (1) 1
anticonvulsants (1) 1
anticonvulsants - adverse effects (1) 1
anticonvulsants - therapeutic use (1) 1
batteries (1) 1
bcects (1) 1
benign (1) 1
benign childhood epilepsy (1) 1
body mass index (1) 1
case report (1) 1
cbcl (1) 1
centrotemporal spikes bects (1) 1
child and adolescent psychiatry (1) 1
child behavior (1) 1
child behavior - physiology (1) 1
child, preschool (1) 1
childhood epilepsy (1) 1
children (1) 1
cognition (1) 1
cognition - drug effects (1) 1
cognition disorders - etiology (1) 1
cognitive ability (1) 1
complications (1) 1
craniocerebral trauma (1) 1
dementia (1) 1
differential diagnosis (1) 1
differenzialdiagnose (1) 1
digestive system (1) 1
double-blind method (1) 1
eeg (1) 1
electroencephalography - methods (1) 1
epidemiology (1) 1
epilepsy, rolandic - drug therapy (1) 1
epilepsy, rolandic - physiopathology (1) 1
executive function (1) 1
firing pattern (1) 1
general practice / family medicine (1) 1
geriatrics (1) 1
gerontology (1) 1
head injuries (1) 1
home health care (1) 1
hospitals (1) 1
ictal kissing (1) 1
idiopathic epilepsy (1) 1
intelligence (1) 1
key subject session (1) 1
kindesmisshandlung (1) 1
kraniozerebrales trauma (1) 1
kss (1) 1
language (1) 1
levetiracetam (1) 1
levetiracetam monotherapy (1) 1
malnutrition (1) 1
medicine & public health (1) 1
memory - drug effects (1) 1
mental recall - drug effects (1) 1
mutations (1) 1
neuropsychological assessment (1) 1
nondominant temporal lobe (1) 1
nurses (1) 1
nursing homes (1) 1
nutrition (1) 1
older people (1) 1
oral presentations (1) 1
oxcarbazepine (1) 1
pediatric epilepsy (1) 1
pediatric surgery (1) 1
performance (1) 1
piracetam - adverse effects (1) 1
piracetam - analogs & derivatives (1) 1
piracetam - therapeutic use (1) 1
prevention (1) 1
prävention (1) 1
psychomotor performance - drug effects (1) 1
public health (1) 1
rolandic epilepsy (1) 1
schütteltrauma-syndrom (1) 1
sleep (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Neuropediatrics, ISSN 0174-304X, 04/2017, Volume 48, Issue S 01, pp. S1 - S45
Conference Proceeding
Monatsschrift Kinderheilkunde, ISSN 0026-9298, 10/2019, Volume 167, Issue 10, pp. 891 - 899
Das Schütteltraumasyndrom (STS), im englischen Sprachgebrauch „abusive head trauma“ (AHT), ist eine klar definierte und gängige medizinische Diagnose, dessen... 
Pediatrics | Prävention | Schütteltrauma-Syndrom | Child and Adolescent Psychiatry | General Practice / Family Medicine | Kraniozerebrales Trauma | Prevention | Child abuse | Medicine & Public Health | Abusive Head Trauma | Differential diagnosis | Kindesmisshandlung | Craniocerebral trauma | Differenzialdiagnose | Pediatric Surgery
Journal Article
Monatsschrift Kinderheilkunde, ISSN 0026-9298, 10/2019, Volume 167, Issue 10, p. 891
Das Schutteltraumasyndrom (STS), im englischen Sprachgebrauch "abusive head trauma" (AHT), ist eine klar definierte und gangige medizinische Diagnose, dessen... 
Child abuse | Head injuries | Analysis | Epidemiology
Journal Article
Neuropediatrics, ISSN 0174-304X, 04/2017, Volume 48, Issue S 01, pp. S1 - S45
Conference Proceeding
Neuropediatrics, ISSN 0174-304X, 09/2014, Volume 45, Issue S 01
Background: The SLC2A1 gene on chromosome 1 encodes a glucose transporter in the blood-brain barrier. A defect of this gene is responsible for the glucose... 
Conference Proceeding
by Tacke, Moritz and Rupp, Nina and Gerstl, Lucia and Heinen, Florian and Vill, Katharina and Bonfert, Michaela and Neubauer, Bernd Axel and Bast, Thomas and Borggraefe, Ingo and Baumeister, F A M and Baethmann, M and Schreiber‐Gollwitzer, B and Bentele, K and Blank, C and Held, J and Blank, H M and Liebrich, K and Bode, H and Braun, J and Bosch, F and Wagner, R and Brandl, U and Wetzel, K and Brockmann, K and Schlockwerder, C and Dahlem, P and Baudler, I and Ernst, J P and Mayer, H and Feldmann, E and Pattber‐Wolff, A and Fiedler, A and Sonnleitner, S and Gerigk, M and Heß, S and Feiereis, T and Hikel, C and Hoffmann, H G and Rickeshenrich, A and Kieslich, M and Dewitz, R and Baz Bartels, M and Klepper, J and Kleuker, S and Kluger, G and Kirsch, A and Koch, H and Meerpohl, U and Koch, W and Korinthenberg, R and Stehle‐Renner, B and Krois, I and Wegener, A and Kühne, H and Weiß, C and Kurlemann, G and Elkemann, U and Mandl, M and Friedl, A and Mause, U and Müller, M and Navratil, P and Iken, U and Opp, J and Walter, J and Penzien, J and Prietsch, V and Siegrist, B and Quattländer, A and Rating, D and Reuner, G and Schara, U and Shamdeen, M G and Struchholz, H and prinz, A and Wendker‐Magrabi, H and Stephani, U and Muhle, H and Carlsson, G and Straßburg, H M and Ottensmeier, H and Töpke, B and Tatsek, K and Trollmann, R and Poida‐Herzing, E and Tuschen‐Hofstätter, E and Menschig, M and Waltz, S and Pickartz, A and Weber, G and Gehnen, T and Wien, F U and Antemann, J and Wolff, M and Serra, E and Polster, T and Freitag, H and Sönmez, Ö and Rheinhardt, K and Traus, M and ... and Further Members German HE and Further Members of the German HEAD Study Group
Acta Neurologica Scandinavica, ISSN 0001-6314, 12/2018, Volume 138, Issue 6, pp. 475 - 481
Journal Article
Journal Article
Neuropediatrics, ISSN 0174-304X, 03/2013, Volume 44, Issue 2
Background: Farber disease (OMIM 228000), a rare autosomal recessive disorder of lipid metabolism. The defect of the lysosomal ceramidase causes an... 
Conference Proceeding
Neuropediatrics, ISSN 0174-304X, 04/2012, Volume 43, Issue 2
Aims: Ataxia Telangiectasia (AT) is an autosomal recessive inherited ataxia and results from a mutation within the ATM (Ataxia Telangiectasia Mutated)-gene.... 
Conference Proceeding
Neuropediatrics, ISSN 0174-304X, 08/2010, Volume 41, Issue 2
Background: The Calpainopathy (LGMD2A; OMIM 253600) is an autosomal-recessive bequeathed disease of the group of genetic determined limb-girdle muscular... 
Conference Proceeding
Neuropediatrics, ISSN 0174-304X, 08/2010, Volume 41, Issue 2
Background information and Case report: CMT-Type 4E, or congenital hypomyelinating neuropathy (CHN) is an extremely rare disorder of myelin formation. Patients... 
Conference Proceeding
Neuropediatrics, ISSN 0174-304X, 08/2010, Volume 41, Issue 2
Pediatric multiple sclerosis (PMS), likely occurring in 0.2–0.6% of all MS cases, has been increasingly recognized in the past 10 years. PMS (<18 years)... 
Conference Proceeding
International journal of legal medicine, ISSN 0937-9827, 03/2020
Mongolian spots (MS) are congenital dermal conditions resulting from neural crest-derived melanocytes migration to the skin during embryogenesis. MS incidences... 
Journal Article
Neuropediatrics, ISSN 0174-304X, 06/2008, Volume 39, Issue 1
Objective: The common sawfish (Pristis pristis) is a sawfish of the family Pristidae, found in subtropical waters up to 5 meters long. His head shows a saw... 
Conference Proceeding
Neuropediatrics, ISSN 0174-304X, 06/2008, Volume 39, Issue 1
Objective: Acute Necrotizing Encephalopathy (ANE) is a description of a diffuse disease of the brain that affects brain function and structure. At present, the... 
Conference Proceeding
Neuropediatrics, ISSN 0174-304X, 06/2008, Volume 39, Issue 1
Aims: The differential diagnosis of „ocular changes and retardation“ in the first year of life is challenging. Further history and clinical informations may... 
Conference Proceeding
Neuropediatrics, ISSN 0174-304X, 06/2008, Volume 39, Issue 1
Introduction: Ifosfamide (IFO), a nitrogen mustard derived alkylating chemotherapeutic agent has been associated with neurotoxicity in 5–33% of treated... 
Conference Proceeding
Neuropediatrics, ISSN 0174-304X, 06/2008, Volume 39, Issue 1
Background: The Lipogranulomatosis (Farber disease, OMIM: 228000) is a rare sphingolipidosis caused by the deficiency of the enzyme ceramidase. This enzyme... 
Conference Proceeding
Neuropediatrics, ISSN 0174-304X, 03/2007, Volume 37, Issue 6
Aims: The idiopathic orbital Myositis is a rare disease. Typical symptoms are retrobulbar pain with painful eye movements, diplopia on deviation of eyeball,... 
Conference Proceeding
Neuropediatrics, ISSN 0174-304X, 03/2007, Volume 37, Issue 6
Aims: Primary pseudotumor cerebri (PTC) is defined as elevated cerebrospinal fluid (CSF) pressure of more than 20cm H2O and exclusion of infectious, structural... 
Conference Proceeding
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.