(Q53580348)

English

3-Methylcrotonyl-coenzyme A carboxylase deficiency in Amish/Mennonite adults identified by detection of increased acylcarnitines in blood spots of their children.

scientific article published in March 1998

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

15 May 2018

http://europepmc.org/abstract/MED/9544913

3-Methylcrotonyl-coenzyme A carboxylase deficiency in Amish/Mennonite adults identified by detection of increased acylcarnitines in blood spots of their children. (English)

1 reference

Europe PubMed Central

PubMed publication ID

15 May 2018

http://europepmc.org/abstract/MED/9544913

0 references

author name string

Gibson KM

1

1 reference

Europe PubMed Central

PubMed publication ID

15 May 2018

http://europepmc.org/abstract/MED/9544913

Bennett MJ

2

1 reference

Europe PubMed Central

PubMed publication ID

15 May 2018

http://europepmc.org/abstract/MED/9544913

Naylor EW

3

1 reference

Europe PubMed Central

PubMed publication ID

15 May 2018

http://europepmc.org/abstract/MED/9544913

Morton DH

4

1 reference

Europe PubMed Central

PubMed publication ID

15 May 2018

http://europepmc.org/abstract/MED/9544913

language of work or name

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publication date

1 March 1998

1 reference

Europe PubMed Central

PubMed publication ID

15 May 2018

http://europepmc.org/abstract/MED/9544913

The Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

15 May 2018

http://europepmc.org/abstract/MED/9544913

132

1 reference

Europe PubMed Central

PubMed publication ID

15 May 2018

http://europepmc.org/abstract/MED/9544913

3 Pt 1

1 reference

Europe PubMed Central

PubMed publication ID

15 May 2018

http://europepmc.org/abstract/MED/9544913

519-523

1 reference

Europe PubMed Central

PubMed publication ID

15 May 2018

http://europepmc.org/abstract/MED/9544913

Isolated biotin‐resistant deficiency of 3‐methylcrotonyl‐CoA carboxylase presenting as a clinically severe form in a newborn with fatal outcome

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970032-0

7 January 2021

Familial hypotonia of childhood caused by isolated 3-methylcrotonyl-coenzyme A carboxylase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970032-0

7 January 2021

Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency presenting as a Reye syndrome-like illness

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970032-0

7 January 2021

Isolated 3‐methylcrotonyl‐CoA carboxylase deficiency in a 16‐month‐old child

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970032-0

7 January 2021

Isolated (biotin-resistant) 3-methylcrotonyl-CoA carboxylase deficiency: four sibs devoid of pathology

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970032-0

7 January 2021

Benign clinical presentation of 3-methylcrotonylglycinuria

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970032-0

7 January 2021

Glycine andl-carnitine therapy in 3-methylcrotonyl-CoA carboxylase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970032-0

7 January 2021

3-Hydroxyisovalerylcarnitine in 3-methylcrotonyl-CoA carboxylase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970032-0

7 January 2021

3-Hydroxyisovalerylcarnitine in patients with deficiency of 3-methylcrotonyl CoA carboxylase

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970032-0

7 January 2021

Identifiers

10.1016/S0022-3476(98)70032-0

1 reference

Europe PubMed Central

PubMed publication ID

15 May 2018

http://europepmc.org/abstract/MED/9544913

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

15 May 2018

http://europepmc.org/abstract/MED/9544913

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