-
Je něco špatně v tomto záznamu ?
258th ENMC international workshop Leigh syndrome spectrum: genetic causes, natural history and preparing for clinical trials 25-27 March 2022, Hoofddorp, Amsterdam, The Netherlands
D. Diodato, M. Schiff, BH. Cohen, E. Bertini, S. Rahman, Workshop participants
Neuromuscular disorders.
2023 ;
33 (8) :
700-709.
[pub] 20230615
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu konzilia, práce podpořená grantem
Perzistentní odkaz
https://www.medvik.cz/link/bmc23016640
- MeSH
- Leighova nemoc * genetika terapie MeSH
- lidé MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- konzilia MeSH
- práce podpořená grantem MeSH
- Geografické názvy
- Nizozemsko MeSH
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc23016640
- 003
- CZ-PrNML
- 005
- 20231026105646.0
- 007
- ta
- 008
- 231013s2023 enk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.nmd.2023.06.002 $2 doi
- 035 __
- $a (PubMed)37541860
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a enk
- 100 1_
- $a Diodato, Daria $u Unit of Neuromuscular and Neurodegenerative Disorders, Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy
- 245 10
- $a 258th ENMC international workshop Leigh syndrome spectrum: genetic causes, natural history and preparing for clinical trials 25-27 March 2022, Hoofddorp, Amsterdam, The Netherlands / $c D. Diodato, M. Schiff, BH. Cohen, E. Bertini, S. Rahman, Workshop participants
- 650 _2
- $a lidé $7 D006801
- 650 12
- $a Leighova nemoc $x genetika $x terapie $7 D007888
- 651 _2
- $a Nizozemsko $7 D009426
- 655 _2
- $a konzilia $7 D016429
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Schiff, Manuel $u Reference Center for Mitochondrial Disease, CARAMMEL, Necker University Hospital, APHP and University of Paris Cité, Paris, France; INSERM UMRS_1163, Institut Imagine, Paris, France
- 700 1_
- $a Cohen, Bruce H $u Department of Pediatrics and Rebecca D. Considine Research Institute, Akron Children's Hospital, Akron, OH, United States
- 700 1_
- $a Bertini, Enrico $u Unit of Neuromuscular and Neurodegenerative Disorders, Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy
- 700 1_
- $a Rahman, Shamima $u Genetics and Genomic Medicine Department, UCL Great Ormond Street Institute of Child Health, London WC1N 1EH, UK and Metabolic Unit, Great Ormond Street Hospital, London WC1N 3JH, United Kingdom. Electronic address: shamima.rahman@ucl.ac.uk
- 710 2_
- $a Workshop participants
- 773 0_
- $w MED00003492 $t Neuromuscular disorders : NMD $x 1873-2364 $g Roč. 33, č. 8 (2023), s. 700-709
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/37541860 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y - $z 0
- 990 __
- $a 20231013 $b ABA008
- 991 __
- $a 20231026105641 $b ABA008
- 999 __
- $a ok $b bmc $g 2000264 $s 1203002
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2023 $b 33 $c 8 $d 700-709 $e 20230615 $i 1873-2364 $m Neuromuscular disorders $n Neuromuscul Disord $x MED00003492
- LZP __
- $a Pubmed-20231013
