Outcome of the glutaric aciduria type 1 (GA1) newborn screening program in Manitoba: 1980-2020

Glutaric aciduria type 1 (GA1) is a severe inherited neurometabolic disorder whose clinical outcome has improved after implementation of newborn screening (NBS) programs and prompt beginning of guideline-directed presymptomatic metabolic treatment. We report the outcome of our 40-year experience wit...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Mhanni, Aziz (VerfasserIn) , Aylward, Nicole (VerfasserIn) , Boy, Nikolas (VerfasserIn) , Martin, Bruce (VerfasserIn) , Sharma, Atul (VerfasserIn) , Rockman-Greenberg, Cheryl (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 25 November 2020
In: Molecular genetics and metabolism reports
Year: 2020, Jahrgang: 25, Pages: 1-3
ISSN:2214-4269
DOI:10.1016/j.ymgmr.2020.100666
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.ymgmr.2020.100666
Verlag, lizenzpflichtig, Volltext: https://www.sciencedirect.com/science/article/pii/S2214426920301129
Volltext
Verfasserangaben:A. Mhanni, N. Aylward, N. Boy, B. Martin, A. Sharma, C. Rockman-Greenberg

MARC

LEADER 00000caa a2200000 c 4500
001 1789517664
003 DE-627
005 20220820130234.0
007 cr uuu---uuuuu
008 220214s2020 xx |||||o 00| ||eng c
024 7 |a 10.1016/j.ymgmr.2020.100666  |2 doi 
035 |a (DE-627)1789517664 
035 |a (DE-599)KXP1789517664 
035 |a (OCoLC)1341441520 
040 |a DE-627  |b ger  |c DE-627  |e rda 
041 |a eng 
084 |a 33  |2 sdnb 
100 1 |a Mhanni, Aziz  |e VerfasserIn  |0 (DE-588)125195944X  |0 (DE-627)1789929040  |4 aut 
245 1 0 |a Outcome of the glutaric aciduria type 1 (GA1) newborn screening program in Manitoba  |b 1980-2020  |c A. Mhanni, N. Aylward, N. Boy, B. Martin, A. Sharma, C. Rockman-Greenberg 
246 3 0 |a one 
264 1 |c 25 November 2020 
300 |a 3 
336 |a Text  |b txt  |2 rdacontent 
337 |a Computermedien  |b c  |2 rdamedia 
338 |a Online-Ressource  |b cr  |2 rdacarrier 
500 |a Gesehen am 17.02.2022 
520 |a Glutaric aciduria type 1 (GA1) is a severe inherited neurometabolic disorder whose clinical outcome has improved after implementation of newborn screening (NBS) programs and prompt beginning of guideline-directed presymptomatic metabolic treatment. We report the outcome of our 40-year experience with the diagnosis and management of GA1 which has improved but remains suboptimal. 
650 4 |a GA1 
650 4 |a Newborn screening 
650 4 |a Outcome 
700 1 |a Aylward, Nicole  |e VerfasserIn  |4 aut 
700 1 |a Boy, Nikolas  |d 1981-  |e VerfasserIn  |0 (DE-588)138823421  |0 (DE-627)606152210  |0 (DE-576)309253659  |4 aut 
700 1 |a Martin, Bruce  |e VerfasserIn  |4 aut 
700 1 |a Sharma, Atul  |e VerfasserIn  |4 aut 
700 1 |a Rockman-Greenberg, Cheryl  |e VerfasserIn  |4 aut 
773 0 8 |i Enthalten in  |t Molecular genetics and metabolism reports  |d Amsterdam [u.a.] : Elsevier, 2014  |g 25(2020), Artikel-ID 100666, Seite 1-3  |h Online-Ressource  |w (DE-627)826105033  |w (DE-600)2821908-9  |w (DE-576)433071052  |x 2214-4269  |7 nnas  |a Outcome of the glutaric aciduria type 1 (GA1) newborn screening program in Manitoba 1980-2020 
773 1 8 |g volume:25  |g year:2020  |g elocationid:100666  |g pages:1-3  |g extent:3  |a Outcome of the glutaric aciduria type 1 (GA1) newborn screening program in Manitoba 1980-2020 
856 4 0 |u https://doi.org/10.1016/j.ymgmr.2020.100666  |x Verlag  |x Resolving-System  |z lizenzpflichtig  |3 Volltext 
856 4 0 |u https://www.sciencedirect.com/science/article/pii/S2214426920301129  |x Verlag  |z lizenzpflichtig  |3 Volltext 
951 |a AR 
992 |a 20220214 
993 |a Article 
994 |a 2020 
998 |g 138823421  |a Boy, Nikolas  |m 138823421:Boy, Nikolas  |d 910000  |d 910500  |d 50000  |e 910000PB138823421  |e 910500PB138823421  |e 50000PB138823421  |k 0/910000/  |k 1/910000/910500/  |k 0/50000/  |p 3 
999 |a KXP-PPN1789517664  |e 4056417024 
BIB |a Y 
SER |a journal 
JSO |a {"person":[{"family":"Mhanni","given":"Aziz","roleDisplay":"VerfasserIn","display":"Mhanni, Aziz","role":"aut"},{"display":"Aylward, Nicole","roleDisplay":"VerfasserIn","role":"aut","family":"Aylward","given":"Nicole"},{"given":"Nikolas","family":"Boy","role":"aut","display":"Boy, Nikolas","roleDisplay":"VerfasserIn"},{"given":"Bruce","family":"Martin","role":"aut","roleDisplay":"VerfasserIn","display":"Martin, Bruce"},{"role":"aut","display":"Sharma, Atul","roleDisplay":"VerfasserIn","given":"Atul","family":"Sharma"},{"family":"Rockman-Greenberg","given":"Cheryl","roleDisplay":"VerfasserIn","display":"Rockman-Greenberg, Cheryl","role":"aut"}],"title":[{"title":"Outcome of the glutaric aciduria type 1 (GA1) newborn screening program in Manitoba","subtitle":"1980-2020","title_sort":"Outcome of the glutaric aciduria type 1 (GA1) newborn screening program in Manitoba"}],"type":{"bibl":"article-journal","media":"Online-Ressource"},"note":["Gesehen am 17.02.2022"],"language":["eng"],"recId":"1789517664","name":{"displayForm":["A. Mhanni, N. Aylward, N. Boy, B. Martin, A. Sharma, C. Rockman-Greenberg"]},"origin":[{"dateIssuedKey":"2020","dateIssuedDisp":"25 November 2020"}],"id":{"doi":["10.1016/j.ymgmr.2020.100666"],"eki":["1789517664"]},"physDesc":[{"extent":"3 S."}],"relHost":[{"origin":[{"publisherPlace":"Amsterdam [u.a.]","dateIssuedDisp":"2014-","dateIssuedKey":"2014","publisher":"Elsevier"}],"id":{"zdb":["2821908-9"],"eki":["826105033"],"issn":["2214-4269"]},"physDesc":[{"extent":"Online-Ressource"}],"title":[{"title":"Molecular genetics and metabolism reports","title_sort":"Molecular genetics and metabolism reports"}],"note":["Gesehen am 25.06.20"],"disp":"Outcome of the glutaric aciduria type 1 (GA1) newborn screening program in Manitoba 1980-2020Molecular genetics and metabolism reports","type":{"bibl":"periodical","media":"Online-Ressource"},"language":["eng"],"recId":"826105033","pubHistory":["1.2014 -"],"part":{"year":"2020","pages":"1-3","volume":"25","text":"25(2020), Artikel-ID 100666, Seite 1-3","extent":"3"},"titleAlt":[{"title":"MGM reports"}]}]} 
SRT |a MHANNIAZIZOUTCOMEOFT2520