Correction to: 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: one disease - many faces

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Notes: Orphanet journal of rare diseases. - 17 (2022) , 16, ISSN: 1750-1172

Event: Veröffentlichung

(where): Freiburg

(who): Universität

(when): 2022

Creator: Grünert, Sarah
Sass, Jörn Oliver

DOI: 10.1186/s13023-021-02154-z

URN: urn:nbn:de:bsz:25-freidok-2240322

Rights: Kein Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:22 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Show original at data provider

Associated

Time of origin

2022

Other Objects (12)

3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: one disease - many faces

Clinical and genetical heterogeneity of late-onset multiple acyl-coenzyme A dehydrogenase deficiency

Hochschulschrift

Organoazidopathien im Blickpunkt des Neugeborenen-Screenings - Wandel des klinischen Phänotyps und kritische Aspekte des Screenings

Hochschulschrift

Isovalerianazidämie : Klinik, Pathobiochemie und Therapie am Beispiel von 28 Patienten

2-methylacetoacetyl-coenzyme A thiolase (beta-ketothiolase) deficiency: one disease - two pathways

Clinical and genetical heterogeneity of late-onset multiple acyl-coenzyme A dehydrogenase deficiency

Efficacy and safety of empagliflozin in glycogen storage disease type Ib: data from an international questionnaire

Neurological outcome in long‐chain hydroxy fatty acid oxidation disorders

3-hydroxy-3-methylglutaryl-coenzyme a lyase deficiency: a case report

3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: one disease - many faces

Clinical and genetical heterogeneity of late-onset multiple acyl-coenzyme A dehydrogenase deficiency

Hochschulschrift

Organoazidopathien im Blickpunkt des Neugeborenen-Screenings - Wandel des klinischen Phänotyps und kritische Aspekte des Screenings

Hochschulschrift

Isovalerianazidämie : Klinik, Pathobiochemie und Therapie am Beispiel von 28 Patienten

2-methylacetoacetyl-coenzyme A thiolase (beta-ketothiolase) deficiency: one disease - two pathways

Clinical and genetical heterogeneity of late-onset multiple acyl-coenzyme A dehydrogenase deficiency

Efficacy and safety of empagliflozin in glycogen storage disease type Ib: data from an international questionnaire

Neurological outcome in long‐chain hydroxy fatty acid oxidation disorders

3-hydroxy-3-methylglutaryl-coenzyme a lyase deficiency: a case report

3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: one disease - many faces

Clinical and genetical heterogeneity of late-onset multiple acyl-coenzyme A dehydrogenase deficiency

Hochschulschrift

Organoazidopathien im Blickpunkt des Neugeborenen-Screenings - Wandel des klinischen Phänotyps und kritische Aspekte des Screenings

Hochschulschrift

Isovalerianazidämie : Klinik, Pathobiochemie und Therapie am Beispiel von 28 Patienten

2-methylacetoacetyl-coenzyme A thiolase (beta-ketothiolase) deficiency: one disease - two pathways

Clinical and genetical heterogeneity of late-onset multiple acyl-coenzyme A dehydrogenase deficiency

Efficacy and safety of empagliflozin in glycogen storage disease type Ib: data from an international questionnaire

Neurological outcome in long‐chain hydroxy fatty acid oxidation disorders

3-hydroxy-3-methylglutaryl-coenzyme a lyase deficiency: a case report

Cultural heritage institutions wishing to register will find more information here.

Fields marked * need to be filled in.

Username*

Please enter your username

Email*

Please enter your email address

Please do not fill this field

First name

Last name

Password*

Please enter your password

Confirm password*

Please enter the same password

I have read the terms of use and the privacy policy for the collection of personal data and accept them. *

This field is required.

I would like to subscribe to the newsletter of the Deutsche Digitale Bibliothek. See newsletter subscription info.

Account created

Your "My DDB" account has been successfully created. Before you can log in to your account, you must click the confirmation link in the message we just sent to the email address you provided.

Correction to: 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: one disease - many faces

Object Details

Contributors, Places and Time

Further information

Data provider

Associated

Time of origin

Other Objects (12)

3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: one disease - many faces

3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: one disease - many faces

3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: one disease - many faces

Clinical and genetical heterogeneity of late-onset multiple acyl-coenzyme A dehydrogenase deficiency

Organoazidopathien im Blickpunkt des Neugeborenen-Screenings - Wandel des klinischen Phänotyps und kritische Aspekte des Screenings

Isovalerianazidämie : Klinik, Pathobiochemie und Therapie am Beispiel von 28 Patienten

2-methylacetoacetyl-coenzyme A thiolase (beta-ketothiolase) deficiency: one disease - two pathways

2-methylacetoacetyl-coenzyme A thiolase (beta-ketothiolase) deficiency: one disease - two pathways

Clinical and genetical heterogeneity of late-onset multiple acyl-coenzyme A dehydrogenase deficiency

Efficacy and safety of empagliflozin in glycogen storage disease type Ib: data from an international questionnaire

Neurological outcome in long‐chain hydroxy fatty acid oxidation disorders

3-hydroxy-3-methylglutaryl-coenzyme a lyase deficiency: a case report

3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: one disease - many faces

3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: one disease - many faces

3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: one disease - many faces

Clinical and genetical heterogeneity of late-onset multiple acyl-coenzyme A dehydrogenase deficiency

Organoazidopathien im Blickpunkt des Neugeborenen-Screenings - Wandel des klinischen Phänotyps und kritische Aspekte des Screenings

Isovalerianazidämie : Klinik, Pathobiochemie und Therapie am Beispiel von 28 Patienten

2-methylacetoacetyl-coenzyme A thiolase (beta-ketothiolase) deficiency: one disease - two pathways

2-methylacetoacetyl-coenzyme A thiolase (beta-ketothiolase) deficiency: one disease - two pathways

Clinical and genetical heterogeneity of late-onset multiple acyl-coenzyme A dehydrogenase deficiency

Efficacy and safety of empagliflozin in glycogen storage disease type Ib: data from an international questionnaire

Neurological outcome in long‐chain hydroxy fatty acid oxidation disorders

3-hydroxy-3-methylglutaryl-coenzyme a lyase deficiency: a case report

3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: one disease - many faces

3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: one disease - many faces

3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: one disease - many faces

Clinical and genetical heterogeneity of late-onset multiple acyl-coenzyme A dehydrogenase deficiency

Organoazidopathien im Blickpunkt des Neugeborenen-Screenings - Wandel des klinischen Phänotyps und kritische Aspekte des Screenings

Isovalerianazidämie : Klinik, Pathobiochemie und Therapie am Beispiel von 28 Patienten

2-methylacetoacetyl-coenzyme A thiolase (beta-ketothiolase) deficiency: one disease - two pathways

2-methylacetoacetyl-coenzyme A thiolase (beta-ketothiolase) deficiency: one disease - two pathways

Clinical and genetical heterogeneity of late-onset multiple acyl-coenzyme A dehydrogenase deficiency

Efficacy and safety of empagliflozin in glycogen storage disease type Ib: data from an international questionnaire

Neurological outcome in long‐chain hydroxy fatty acid oxidation disorders

3-hydroxy-3-methylglutaryl-coenzyme a lyase deficiency: a case report

Related objects

Reset password