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Person

Nils Janzen (1963-)

Arzt

Name	Nils Janzen
Time	1963- (Date of birth and death)
Place	Bochum (Wirkungsort) Bad Sülze (Mecklenburg-Vorpommern) (Geburtsort) Deutschland
Academic degree	Dr. rer. nat., Dr. med.
Profession	Arzt (characteristic profession) Biochemiker
Related	Helios-St.-Josefs-Hospital (Bochum)
Further information	1. Diss. an der Universität Hannover (1995); 2. Diss. an der Medizinischen Hochschule Hannover (2009)
Record type	Person
GND-Identifier	114348472
Record ID	114348472
Involved in show all Diagnosis, treatment, management and monitoring of patients with tyrosinaemia type 1: consensus group recommendations from the German‐speaking countries Functional characterization of MARCKS-associated immunological processes in the monocytic cell type Infants with biliary atresia exhibit an altered amino acid profile in their newborn screening Entwicklung der Analytik im Neugeborenen-Screening – Von der Guthrie-Karte zur Genetik High Throughput Newborn Screening for Sickle Cell Disease – Application of Two-Tiered Testing with a qPCR-Based Primary screen Collaborative evaluation study on 18 candidate diseases for newborn screening in 1.77 million samples Sudden neonatal death in individuals with medium-chain acyl-coenzyme A dehydrogenase deficiency: limit of newborn screening The First 4 Years – Outcome of Children Identified by Newborn Screening for CF in Germany Nitisinone treatment during two pregnancies and breastfeeding in a woman with tyrosinemia type 1 – a case report Methionine adenosyltransferase I/III deficiency detected by newborn screening A newborn screening approach to diagnose 3‐hydroxy‐3‐methylglutaryl‐CoA lyase deficiency Molecular based newborn screening in Germany: follow-up for cystinosis Non-invasive test using palmitate in patients with suspected fatty acid oxidation defects: disease-specific acylcarnitine patterns can help to establish the diagnosis Lipopolysaccharides and Prematurity: Effect on the Activity of Respiratory Chain Enzymes in Human Umbilical Venous Endothelial Cells Macro-AST: misleading finding in an adolescent with MCAD-deficiency Neonatal screening: identification of children with 11β-hydroxylase deficiency by second-tier testing Energy metabolism in umbilical endothelial cells from preterm and term neonates Tandemmassenspektrometrische Bestimmung von Steroid-Hormonen zur Früherkennung und Differentialdiagnose des adrenogenitalen Syndroms Neonatal screening for citrullinaemia Neonatal screening for medium chain acyl-CoA deficiency: high incidence in Lower Saxony (northern Germany) Tandemmassenspektrometrie Beitrag zum Neugeborenenscreening auf angeborene Störungen des Stoffwechsels : Beitrag zum Neugeborenenscreening auf angeborene Störungen des Stoffwechsels Untersuchung der humanen Adenin-Phosphoribosyltransferase : Enzymcharakterisierung und Enzymaktivität in Erythrozyten sowie Bestimmung von Metaboliten des Purinstoffwechsels in Blut und Urin

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Katalog der Deutschen Nationalbibliothek

Nils Janzen (1963-)

Diagnosis, treatment, management and monitoring of patients with tyrosinaemia type 1: consensus group recommendations from the German‐speaking countries

Functional characterization of MARCKS-associated immunological processes in the monocytic cell type

Infants with biliary atresia exhibit an altered amino acid profile in their newborn screening

Entwicklung der Analytik im Neugeborenen-Screening – Von der Guthrie-Karte zur Genetik

High Throughput Newborn Screening for Sickle Cell Disease – Application of Two-Tiered Testing with a qPCR-Based Primary screen

Collaborative evaluation study on 18 candidate diseases for newborn screening in 1.77 million samples

Sudden neonatal death in individuals with medium-chain acyl-coenzyme A dehydrogenase deficiency: limit of newborn screening

The First 4 Years – Outcome of Children Identified by Newborn Screening for CF in Germany

Nitisinone treatment during two pregnancies and breastfeeding in a woman with tyrosinemia type 1 – a case report

Methionine adenosyltransferase I/III deficiency detected by newborn screening

A newborn screening approach to diagnose 3‐hydroxy‐3‐methylglutaryl‐CoA lyase deficiency

Molecular based newborn screening in Germany: follow-up for cystinosis

Non-invasive test using palmitate in patients with suspected fatty acid oxidation defects: disease-specific acylcarnitine patterns can help to establish the diagnosis

Lipopolysaccharides and Prematurity: Effect on the Activity of Respiratory Chain Enzymes in Human Umbilical Venous Endothelial Cells

Macro-AST: misleading finding in an adolescent with MCAD-deficiency

Neonatal screening: identification of children with 11β-hydroxylase deficiency by second-tier testing

Energy metabolism in umbilical endothelial cells from preterm and term neonates

Tandemmassenspektrometrische Bestimmung von Steroid-Hormonen zur Früherkennung und Differentialdiagnose des adrenogenitalen Syndroms

Neonatal screening for citrullinaemia

Neonatal screening for medium chain acyl-CoA deficiency: high incidence in Lower Saxony (northern Germany)

Tandemmassenspektrometrie Beitrag zum Neugeborenenscreening auf angeborene Störungen des Stoffwechsels : Beitrag zum Neugeborenenscreening auf angeborene Störungen des Stoffwechsels

Untersuchung der humanen Adenin-Phosphoribosyltransferase : Enzymcharakterisierung und Enzymaktivität in Erythrozyten sowie Bestimmung von Metaboliten des Purinstoffwechsels in Blut und Urin