8 results on '"Shamdeen GM"'
Search Results
2. Non-ketotic hyperglycinemia as a cause for respiratory failure in a newborn
- Author
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Meyer, S, primary, Shamdeen, GM, additional, Gortner, L, additional, and Haas, D, additional
- Published
- 2010
- Full Text
- View/download PDF
3. Sudden unexpected death in epilepsy (SUDEP) bei Kindern: Die Bedeutung der rechtseitigen Inselregion
- Author
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Meyer, S, primary, Shamdeen, GM, additional, and Strittmatter, M, additional
- Published
- 2008
- Full Text
- View/download PDF
4. Diagnostic approach to children with minor traumatic brain injury.
- Author
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Oster I, Shamdeen GM, Ziegler K, Eymann R, Gortner L, and Meyer S
- Subjects
- Adolescent, Algorithms, Brain Concussion diagnosis, Brain Concussion therapy, Child, Child, Preschool, Echoencephalography statistics & numerical data, Female, Germany, Health Services Research, Humans, Infant, Magnetic Resonance Imaging statistics & numerical data, Male, Monitoring, Physiologic statistics & numerical data, Patient Admission statistics & numerical data, Prognosis, Signal Processing, Computer-Assisted, Surveys and Questionnaires, Tomography, X-Ray Computed statistics & numerical data, Utilization Review statistics & numerical data, Brain Injuries diagnosis, Brain Injuries therapy, Diagnostic Imaging statistics & numerical data, Electroencephalography statistics & numerical data, Glasgow Coma Scale statistics & numerical data, Head Injuries, Closed diagnosis, Head Injuries, Closed therapy, Neurologic Examination statistics & numerical data
- Abstract
Study Purpose: To analyse the management of minor traumatic brain injury (MTBI) in paediatric hospitals in Germany., Methods: An electronic survey was sent to 72 children hospitals., Results: All participating (45/72; 62.5 %) hospitals had facilities to perform an electroencephalogram (EEG), 98 % cranial ultrasonography, 94 % MRI studies, and 87 % a CT scan. The initial Glasgow Coma Scale, the clinical presentation/neurological deficits, the intensity of the trauma and external/visible injuries were most important for initial assessment. The main reason for in-patient monitoring was initial clinical neurologic presentation (44 %). X-ray scans were used routinely in only 2.2 %, cMRI scans in 6.7 % and cCT scans in 13.3 %; approximately one third employed ultrasonography. In 22.2 % was an EEG part of the routine diagnostic work-up. Inpatient monitoring for 24-48 h was done in 80 %., Conclusions: Children with MTBI are often monitored clinically without resorting to potentially harmful and expensive diagnostic procedures (cCT scans).
- Published
- 2012
- Full Text
- View/download PDF
5. Electroencephalogram in children with minor traumatic brain injury.
- Author
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Oster I, Shamdeen GM, Gottschling S, Gortner L, and Meyer S
- Subjects
- Adolescent, Brain Injuries etiology, Brain Injuries physiopathology, Child, Child, Preschool, Female, Germany, Hospitalization, Humans, Infant, Infant, Newborn, Male, Retrospective Studies, Brain Injuries diagnosis, Electroencephalography, Trauma Severity Indices
- Abstract
Background: Mild traumatic brain injury (MTBI) is one of the most frequent causes for hospitalisation in childhood. Because of different guidelines in the management the diagnostic approach varies substantially. Apart from neuroimaging studies (CT, MRI, sonography) an electroencephalogram (EEG) is often performed without any evidence-based data supporting its use., Methods: Retrospective analysis of 150 children with MTBI (age 0-16 years), who were admitted to the Children's Hospital of the University of Saarland from January 2006 to December 2007., Results: Mean age was 4.3 (SD 3.6) years: 55.3% were boys. The most common mechanisms of injury were: Minor fall <1 m of height (60%) and fall >1.5 m of height (10%). The most common symptoms were: one or more episodes of vomiting (60%), somnolence (26.7%) and headache (12.7%). On 118 patients an EEG was performed; 106 (89.8%) were normal, 11 (9.3%) pathological and 1 (0.9%) invalid because of artefacts. The pathological EEGs showed focal findings with localised slowing in nine cases, spike-wave complexes in one case and general slowing in one case. Of the 11 patients with pathological EEG, two had a CT scan, two a MRI and two had cranial sonography; all the neuro-imaging was normal. None of the children required neurosurgical intervention, had a negative outcome or showed persistent symptoms., Conclusion: The routine performance of an EEG after MTBI in children is not indicated because in most of the cases it is unrevealing, and may lead to unnecessary diagnostic procedures. Instead, children with MTBI should be closely monitored for possible clinical complications and neurological deterioration.
- Published
- 2010
- Full Text
- View/download PDF
6. Laser acupuncture in children with headache: a double-blind, randomized, bicenter, placebo-controlled trial.
- Author
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Gottschling S, Meyer S, Gribova I, Distler L, Berrang J, Gortner L, Graf N, and Shamdeen GM
- Subjects
- Acupuncture instrumentation, Adolescent, Age Factors, Child, Double-Blind Method, Female, Humans, Laser Therapy instrumentation, Male, Pain Measurement radiation effects, Placebo Effect, Placebos, Prospective Studies, Treatment Outcome, Acupuncture methods, Aging physiology, Headache Disorders therapy, Laser Therapy methods
- Abstract
To investigate whether laser acupuncture is efficacious in children with headache and if active laser treatment is superior to placebo laser treatment in a prospective, randomized, double-blind, placebo-controlled trial of low level laser acupuncture in 43 children (mean age (SD) 12.3 (+/-2.6) years) with headache (either migraine (22 patients) or tension type headache (21 patients)). Patients were randomized to receive a course of 4 treatments over 4 weeks with either active or placebo laser. The treatment was highly individualised based on criteria of Traditional Chinese medicine (TCM). The primary outcome measure was a difference in numbers of headache days between baseline and the 4 months after randomization. Secondary outcome measures included a change in headache severity using a 10 cm Visual Analogue Scale (VAS) for pain and a change in monthly hours with headache. Measurements were taken during 4 weeks before randomization (baseline), at weeks 1-4, 5-8, 9-12 and 13-16 from baseline. The mean number of headaches per month decreased significantly by 6.4 days in the treated group (p<0.001) and by 1.0 days in the placebo group (p=0.22). Secondary outcome measures headache severity and monthly hours with headache decreased as well significantly at all time points compared to baseline (p<0.001) and were as well significantly lower than those of the placebo group at all time points (p<0.001). We conclude that laser acupuncture can provide a significant benefit for children with headache with active laser treatment being clearly more effective than placebo laser treatment.
- Published
- 2008
- Full Text
- View/download PDF
7. Novel POMGnT1 mutations define broader phenotypic spectrum of muscle-eye-brain disease.
- Author
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Hehr U, Uyanik G, Gross C, Walter MC, Bohring A, Cohen M, Oehl-Jaschkowitz B, Bird LM, Shamdeen GM, Bogdahn U, Schuierer G, Topaloglu H, Aigner L, Lochmüller H, and Winkler J
- Subjects
- Adolescent, Animals, Base Sequence, Child, Child, Preschool, Cobblestone Lissencephaly pathology, DNA genetics, Dystroglycans metabolism, Female, Genes, Recessive, Genotype, Heterozygote, Homozygote, Humans, Infant, Male, Mice, Mice, Knockout, Muscular Dystrophies congenital, Muscular Dystrophies pathology, Mutation, Missense, N-Acetylglucosaminyltransferases chemistry, N-Acetylglucosaminyltransferases deficiency, Phenotype, Syndrome, Cobblestone Lissencephaly enzymology, Cobblestone Lissencephaly genetics, Eye Abnormalities enzymology, Eye Abnormalities genetics, Muscular Dystrophies enzymology, Muscular Dystrophies genetics, Mutation, N-Acetylglucosaminyltransferases genetics
- Abstract
Muscle-eye-brain disease (MEB, OMIM 253280) is an autosomal recessive disorder characterized by a distinct triad of congenital muscular dystrophy, structural eye abnormalities, and cobblestone lissencephaly. Clinically, MEB patients present with early onset muscular hypotonia, severely compromised motor development, and mental retardation. Magnetic resonance imaging reveals a lissencephaly type II with hypoplasia of the brainstem and cerebellum. MEB is associated with mutations in the gene for protein O-mannose beta-1,2-N-acetylglucosaminyltransferase (POMGnT1, OMIM 606822). In this paper, we report the clinical findings of nine MEB patients from eight families. Eight of the nine patients presented typical features of MEB. However, a broad phenotypic variability was observed, ranging from two patients with severe autistic features to another patient with an unusually mild phenotype, initially diagnosed as congenital muscular dystrophy. Furthermore, severe hydrocephalus was reported in two families during a previous pregnancy, emphasizing the phenotypic overlap with Walker-Warburg syndrome. In addition to three previously reported mutations, we identified six novel POMGnT1 mutations (one missense, five truncating) in the present patient cohort. Our data suggest mutational hotspots within the minimal catalytic domain at arginine residue 442 (exon 16) and in intron 17. It is interesting to note that all mutations analyzed so far result in a complete loss of enzyme activity. Therefore, we conclude that the type and position of the POMGnT1 mutations are not of predictive value for the clinical severity. This supports the notion that additional environmental and/or genetic factors may contribute to the observed broad spectrum of POMGnT1-associated phenotypes.
- Published
- 2007
- Full Text
- View/download PDF
8. Effects of short-term propofol administration on pancreatic enzymes and triglyceride levels in children.
- Author
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Gottschling S, Meyer S, Krenn T, Kleinschmidt S, Reinhard H, Graf N, and Shamdeen GM
- Subjects
- Adolescent, Amylases blood, Anesthetics, Intravenous pharmacology, Body Weight, Child, Child, Preschool, Conscious Sedation methods, Drug Administration Schedule, Female, Humans, Infant, Lipase blood, Magnetic Resonance Imaging, Male, Prospective Studies, Hypnotics and Sedatives pharmacology, Pancreas drug effects, Pancreas enzymology, Propofol pharmacology, Triglycerides blood
- Abstract
This prospective, clinical trial evaluated the effects of short-term propofol administration on triglyceride levels and serum pancreatic enzymes in children undergoing sedation for magnetic resonance imaging. Laboratory parameters of 40 children, mean age (SD; range) 67 (66; 4-178) months undergoing short-term sedation were assessed before and 4 h after having received propofol. Mean (SD) propofol loading dose was 2.2 (1.1) mg.kg(-1) followed by continuous propofol infusion of 6.9 (0.9) mg.kg(-1).h(-1). Serum lipase levels (p = 0.035) and serum triglyceride levels (p = 0.003) were raised significantly after propofol administration but remained within normal limits. No significant changes in serum pancreatic-amylase levels were seen (p = 0.127). In two (5%) children, pancreatic enzymes and in four (10%) children triglyceride levels were raised above normal limits; however, no child showed clinical symptoms of pancreatitis. We conclude that even short-term propofol administration with standard doses of propofol may have a significant effect on serum triglyceride and pancreatic enzyme levels in children.
- Published
- 2005
- Full Text
- View/download PDF
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