Neslihan Onenli Mungan Selected Research

Acidosis

3/2018

Twenty-seven mutations with three novel pathologenic variants causing biotinidase deficiency: a report of 203 patients from the southeastern part of Turkey.

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Neslihan Onenli Mungan Research Topics

Disease

1	Pelger-Huet Anomaly 01/2020
1	Liver Failure 01/2020
1	Optic Atrophy 01/2020
1	Ketosis 03/2018
1	Acidosis 03/2018
1	Gastroenteritis 03/2018
1	Abetalipoproteinemia (Bassen Kornzweig Syndrome) 01/2016
1	Failure to Thrive 01/2016
1	Chylomicron retention disease 01/2016
1	Hypobetalipoproteinemias (Hypobetalipoproteinemia) 01/2016
1	Respiratory Insufficiency (Respiratory Failure) 05/2015
1	Seizures (Absence Seizure) 05/2015
1	Nonketotic Hyperglycinemia 05/2015
1	Multiple Sulfatase Deficiency Disease (Mucosulfatidosis) 10/2013
1	Type 1 Diabetes Mellitus (Autoimmune Diabetes) 12/2012
1	Rubella (German Measles) 01/2003

Drug/Important Bio-Agent (IBA)

2	LipidsIBA 01/2016 - 10/2013
1	Proteins (Proteins, Gene)FDA Link 01/2020
1	Biotin (Vitamin H)FDA Link 03/2018
1	LDL Lipoproteins (beta Lipoproteins)IBA 01/2016
1	ApolipoproteinsIBA 01/2016
1	Apolipoproteins B (ApoB)IBA 01/2016
1	ChylomicronsIBA 01/2016
1	Peptides (Polypeptides)IBA 01/2016
1	glycine cleavage systemIBA 05/2015
1	Glycine (Aminoacetic Acid)FDA LinkGeneric 05/2015
1	GlycosaminoglycansIBA 10/2013
1	AcidsIBA 10/2013
1	Insulin (Novolin)FDA Link 12/2012
1	ChromiumIBA 12/2012
1	EnzymesIBA 01/2003
1	Immunoglobulin G (IgG)IBA 01/2003