Human head and neck Leigh disease

Appendix e-1: PubMed Search TermsAppendix e-1: PubMed Search Terms
And ("infant"[Mesh terms] or "child"[Mesh terms] or "adolescent"[Mesh terms] or "infant" or "adolescence" or "teenager" or "youth" or "children" or "child" or “baby” or “childhood” or “newborn period” or “preschool child” or “toddler”). Leigh disease
0.52 Mb. 8
read
Syndromes That Cause DeafblindnessSyndromes That Cause Deafblindness
Leigh disease
99.8 Kb. 1
read
Mri in paediatric inherited metabolic brain disordersMri in paediatric inherited metabolic brain disorders
Sudha Bindu Tirumani1, Raghavendra Prasad Y2, Vijaya Kumari Mudunoor3, Suman Chandra Aemjal4. Leigh disease
0.52 Mb. 3
read
Central hypoventilation syndrome Jean-Paul Praud Departments of Pediatrics and Physiology Université de SherbrookeCentral hypoventilation syndrome Jean-Paul Praud Departments of Pediatrics and Physiology Université de Sherbrooke
Rapid Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation (rohhad), Chiari malformation, Prader-Willi syndrome, familial dysautonomia, achondroplasia and Leigh’s disease. Leigh disease
38.59 Kb. 1
read
Syndrome (1 key word/video)Syndrome (1 key word/video)
Leigh disease
98.16 Kb. 1
read
A. Mendelian Band Name of Disorder Gene Symbols mim#A. Mendelian Band Name of Disorder Gene Symbols mim#
Hyperlipoproteinemia, type III apoe 107741 Sea-blue histiocyte disease, 269600 apoe 107741. Leigh disease
18.43 Kb. 1
read
Phenotypic diversity associated with the mt-tv gene m. 1644G>A mutation, a matter of quantityPhenotypic diversity associated with the mt-tv gene m. 1644G>A mutation, a matter of quantity
Matthew j fraidakisa,1, Claude Jardelb,c, Stéphane Allouched, Isabelle Nelsone, Karine Auréc,f, Abdelhamid Slamag, Isabelle Lemièreb, Jean Philippe Theninth, Jean Baptiste Hamoni, Fabien Zagnolij, Delphine Heronk, Frédéric Sedela, Anne. Leigh disease
69.13 Kb. 1
read

  1


The database is protected by copyright ©dentisty.org 2016
send message

    Main page