Ina Knerr - AILBRY - Article Search

Results for 'Ina Knerr' :

Does defective hypoxia signalling cause type 2 diabetes?

Publication Year: 2006

DOI: https://doi.org/10.1530/eje.1.02150

Abstract:

Authors:
- Jörg Dötsch
- Ina Knerr
- Wolfgang Rascher
- Udo Meißner
Population spectrum ofACADMgenotypes correlated to biochemical phenotypes in newborn screening for medium-chain acyl-CoA dehydrogenase deficiency

Publication Year: 2005

DOI: https://doi.org/10.1002/humu.20163

Abstract:

Authors:
- Esther M. Maier
- Bernhard Liebl
- Wulf Röschinger
- U Nennstiel‐Ratzel
- Ralph Fingerhut
- Bernhard Olgemöller
- Ulrich Busch
- Nils Krone
- Rüdiger von Kries
- Adelbert A. Roscher
Neonatal Screening for Very Long-Chain Acyl-CoA Dehydrogenase Deficiency: Enzymatic and Molecular Evaluation of Neonates With Elevated C14:1-Carnitine Levels

Publication Year: 2006

DOI: https://doi.org/10.1542/peds.2006-0666

Abstract:

Authors:
- Michaela Liebig
- Ina Schymik
- Martina Mueller
- U. Wendel
- Ertan Mayatepek
- Jos P.N. Ruiter
- Arnold W. Strauss
- Ronald J. A. Wanders
- Ute Spiekerkoetter
Synergistic effects of hypoxia and insulin are regulated by different transcriptional elements of the human leptin promoter

Publication Year: 2003

DOI: https://doi.org/10.1016/s0006-291x(03)00401-7

Abstract:

Authors:
- Udo Meißner
- Iris Östreicher
- Ida Allabauer
- Wolfgang Rascher
- Jörg Dötsch
A SEPSECS mutation in a 23‐year‐old woman with microcephaly and progressive cerebellar ataxia

Publication Year: 2018

DOI: https://doi.org/10.1007/s10545-018-0151-x

Abstract:

Authors:
- Tessa van Dijk
- Jan‐Dirk Vermeij
- Silvana van Koningsbruggen
- Phillis Lakeman
- Frank Baas
- Bwee Tien Poll‐The
Communicating the benefits and harms of treatments

Publication Year: 2008

DOI: https://doi.org/10.1136/adc.2008.137083

Abstract:

Authors:
- Anthony K Akobeng
IgG N-Glycosylation Galactose Incorporation Ratios for the Monitoring of Classical Galactosaemia

Publication Year: 2015

DOI: https://doi.org/10.1007/8904_2015_490

Abstract:

Authors:
- Henning Stöckmann
- Karen P. Coss
- M. Estela Rubio‐Gozalbo
- Ina Knerr
- Maria Fitzgibbon
- Ashwini Maratha
- James F. Wilson
- Pauline M. Rudd
- Eileen P. Treacy
Plasma methionine concentrations and incidence of hypermethioninemic encephalopathy during infancy in a large cohort of 36 patients with classical homocystinuria in the Republic of Ireland

Publication Year: 2019

DOI: https://doi.org/10.1002/jmd2.12029

Abstract:

Authors:
- John Allen
- Bronwyn Power
- Aida Abedin
- Orla Purcell
- Ina Knerr
- Ahmad Monavari
Oxygen and Trophoblast Behaviour—A Workshop Report

Publication Year: 2004

DOI: https://doi.org/10.1016/j.placenta.2004.01.025

Abstract:

Authors:
- Charles H. Graham
- Graham J. Burton
P411 A systematic approach to health related problems and hand dominance in all children with special needs in the special schools, in magnesia county, greece

Publication Year: 2019

DOI: https://doi.org/10.1136/archdischild-2019-epa.757

Abstract:

Authors:
- Anastasia-Anastasiou Katsiardani
- Konstantinos Katsiardanis
- Zoi Korka
- Kalliopi-Pinelopi Katsiardani
A multinational study of acute and long‐term outcomes of Type 1 galactosemia patients who carry the <scp>S135L</scp> (c.<scp>404C</scp> > T) variant of <scp>GALT</scp>

Publication Year: 2022

DOI: https://doi.org/10.1002/jimd.12556

Abstract:

Authors:
- Quinton S. Katler
- Karolina M. Stępień
- Nathan Paull
- S. G. Patel
- Michael W. W. Adams
- Mehmet Cihan Balcı
- Gerard T. Berry
- Annet M. Bosch
- Angela DeLaO
- Didem Demirbas
- Julianna Edman
- Can Fıçıcıoğlu
- Mélanie Le Goff
- Stephanie Hacker
- Ina Knerr
- Kristen Lancaster
- Hong Li
- Bryce A. Mendelsohn
- Brandi Nichols
- Wladimir Bocca Vieira de Rezende Pinto
- Júlio César Rocha
- M. Estela Rubio‐Gozalbo
- Michael Saad‐Naguib
- Sabine Scholl‐Buergi
- Sarah Searcy
- Paulo Victor Sgobbi de Souza
- Angela Wittenauer
- Judith L. Fridovich‐Keil
GP222 Clinical and metabolic parameters in girls-carriers of LEPR rs1137100 with android and gynoid obesity

Publication Year: 2019

DOI: https://doi.org/10.1136/archdischild-2019-epa.281

Abstract:

Authors:
- Екатерина Шенеман
- Т. А. Баирова
- Kseniia Ievleva
- Л. В. Рычкова
- О. В. Бугун
Rare Metabolic Syndromes, a Vascular Hypotheses of Alzheimer's Disease, and Drug Developments for Attention and Trauma

Publication Year: 2008

DOI: https://doi.org/10.1017/s1092852900016801

Abstract:

Authors:
- Eric Hollander
GP59 A rare cause of ‘mitochondrial disorder’: cockayne syndrome

Publication Year: 2019

DOI: https://doi.org/10.1136/archdischild-2019-epa.125

Abstract:

Authors:
- Arie Fisher
- Muhammad Asghar
- Stephanie Ryan
- Bryan Lynch
- Andrew Green
- Ina Knerr
A Retrospective Chart Review and Infant Feeding Survey in the Irish Phenylketonuria (PKU) Population (2016–2020)

Publication Year: 2023

DOI: https://doi.org/10.20944/preprints202306.2036.v1

Abstract:

Authors:
- Jane Rice
- Jenny McNulty
- Meabh O’Shea
- Teresa Gudex
- Ina Knerr

Found 27 results in 0.107 seconds

What is Boolean Searches

Including any of the words AND, OR, or NOT in any of your searches will enable boolean search. Those words must be UPPERCASE. You can use this in all searches, including using the search parameter, and using search filters.

This allows you to craft complex queries using those boolean operators along with parentheses and quotation marks. Surrounding a phrase with quotation marks will search for an exact match of that phrase, after stemming and stop-word removal (be sure to use double quotation marks — "). Using parentheses will specify order of operations for the boolean operators. Words that are not separated by one of the boolean operators will be interpreted as AND.

Behind the scenes, the boolean search is using Elasticsearch's query string query on the searchable fields (such as title, abstract, and fulltext for works; see each individual entity page for specifics about that entity). Wildcard and fuzzy searches using *, ? or ~ are not allowed; these characters will be removed from any searches. These searches, even when using quotation marks, will go through the same cleaning as described above, including stemming and removal of stop words.

Example Search

Search for works that mention "elmo" and "sesame street", but not the words "cookie" or "monster":

AILBRY - Article Search

Results for 'Ina Knerr' :

Does defective hypoxia signalling cause type 2 diabetes?

Population spectrum of<i>ACADM</i>genotypes correlated to biochemical phenotypes in newborn screening for medium-chain acyl-CoA dehydrogenase deficiency

Neonatal Screening for Very Long-Chain Acyl-CoA Dehydrogenase Deficiency: Enzymatic and Molecular Evaluation of Neonates With Elevated C14:1-Carnitine Levels

Synergistic effects of hypoxia and insulin are regulated by different transcriptional elements of the human leptin promoter

A <i>SEPSECS</i> mutation in a 23‐year‐old woman with microcephaly and progressive cerebellar ataxia

Communicating the benefits and harms of treatments

IgG N-Glycosylation Galactose Incorporation Ratios for the Monitoring of Classical Galactosaemia

Plasma methionine concentrations and incidence of hypermethioninemic encephalopathy during infancy in a large cohort of 36 patients with classical homocystinuria in the Republic of Ireland

Oxygen and Trophoblast Behaviour—A Workshop Report

P411 A systematic approach to health related problems and hand dominance in all children with special needs in the special schools, in magnesia county, greece

A multinational study of acute and long‐term outcomes of Type 1 galactosemia patients who carry the <scp>S135L</scp> (c.<scp>404C</scp> > T) variant of <scp><i>GALT</i></scp>

GP222 Clinical and metabolic parameters in girls-carriers of LEPR rs1137100 with android and gynoid obesity

Rare Metabolic Syndromes, a Vascular Hypotheses of Alzheimer's Disease, and Drug Developments for Attention and Trauma

GP59 A rare cause of ‘mitochondrial disorder’: cockayne syndrome

A Retrospective Chart Review and Infant Feeding Survey in the Irish Phenylketonuria (PKU) Population (2016–2020)

What is Boolean Searches

Example Search

AILBRY - Article Search

Results for 'Ina Knerr' :

Does defective hypoxia signalling cause type 2 diabetes?

Population spectrum of<i>ACADM</i>genotypes correlated to biochemical phenotypes in newborn screening for medium-chain acyl-CoA dehydrogenase deficiency

Neonatal Screening for Very Long-Chain Acyl-CoA Dehydrogenase Deficiency: Enzymatic and Molecular Evaluation of Neonates With Elevated C14:1-Carnitine Levels

Synergistic effects of hypoxia and insulin are regulated by different transcriptional elements of the human leptin promoter

A <i>SEPSECS</i> mutation in a 23‐year‐old woman with microcephaly and progressive cerebellar ataxia

Communicating the benefits and harms of treatments

IgG N-Glycosylation Galactose Incorporation Ratios for the Monitoring of Classical Galactosaemia

Plasma methionine concentrations and incidence of hypermethioninemic encephalopathy during infancy in a large cohort of 36 patients with classical homocystinuria in the Republic of Ireland

Oxygen and Trophoblast Behaviour—A Workshop Report

P411 A systematic approach to health related problems and hand dominance in all children with special needs in the special schools, in magnesia county, greece

A multinational study of acute and long‐term outcomes of Type 1 galactosemia patients who carry the <scp>S135L</scp> (c.<scp>404C</scp> &gt; T) variant of <scp><i>GALT</i></scp>

GP222 Clinical and metabolic parameters in girls-carriers of LEPR rs1137100 with android and gynoid obesity

Rare Metabolic Syndromes, a Vascular Hypotheses of Alzheimer's Disease, and Drug Developments for Attention and Trauma

GP59 A rare cause of ‘mitochondrial disorder’: cockayne syndrome

A Retrospective Chart Review and Infant Feeding Survey in the Irish Phenylketonuria (PKU) Population (2016–2020)

What is Boolean Searches

Example Search

A multinational study of acute and long‐term outcomes of Type 1 galactosemia patients who carry the <scp>S135L</scp> (c.<scp>404C</scp> > T) variant of <scp><i>GALT</i></scp>