UB Paderborn / Katalog / Suche / in CDI

Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology, 2016-02, Vol.14 (1), p.79-87

2016

Link zum Volltext

Verfügbarkeit prüfen

Clinical characteristics of cytochrome P450 oxidoreductase deficiency: a nationwide survey in Japan

Endocrine Journal, 2020, Vol.67(8), pp.853-857

2020

Link zum Volltext

Verfügbarkeit prüfen

GDF15 is a novel biomarker to evaluate efficacy of pyruvate therapy for mitochondrial diseases

Mitochondrion, 2015-01, Vol.20, p.34-42

2015

Link zum Volltext

Verfügbarkeit prüfen

An exploratory study to identify neonatal arterial ischemic stroke: A single-center study

Brain & development (Tokyo. 1979), 2022-11, Vol.44 (10), p.672-680

2022

Link zum Volltext

Verfügbarkeit prüfen

Laryngotracheal separation surgery in a patient with severe Angelman syndrome involving a 19.3 Mb deletion on 15q11.2–q14

Clinical case reports, 2022-11, Vol.10 (11), p.n/a

2022

Link zum Volltext

Verfügbarkeit prüfen

Congenital Hypothyroidism Due to Truncating PAX8 Mutations: A Case Series and Molecular Function Studies

The journal of clinical endocrinology and metabolism, 2020-11, Vol.105 (11), p.1-e4065

2020

Link zum Volltext

Verfügbarkeit prüfen

Molecular pathology of MELAS and l-arginine effects

Biochimica et biophysica acta, 2012-05, Vol.1820 (5), p.608-614

2012

Link zum Volltext

Verfügbarkeit prüfen

Anorexia Nervosa during Adolescence Is Associated with Decreased Gray Matter Volume in the Inferior Frontal Gyrus

PloS one, 2015-06, Vol.10 (6), p.e0128548-e0128548

2015

Link zum Volltext

Verfügbarkeit prüfen

Urinary stone in a 12-year-old adolescent with new-onset type 1 diabetes and diabetic ketoacidosis

Clinical Pediatric Endocrinology, 2022, Vol.31(3), pp.199-204

2022

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 72

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(60)
Mit Volltextzugriff
(68)

Publikationsform

Artikel
(67)
Berichte
(5)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Endothelial dysfunction in MELAS improved by l-arginine supplementation

L-arginine improves the symptoms of strokelike episodes in MELAS

Effects of L-arginine on the acute phase of strokes in three patients with MELAS

Somatic Progenitor Cell Vulnerability to Mitochondrial DNA Mutagenesis Underlies Progeroid Phenotypes in Polg Mutator Mice

Natural course of melas in Japanese cohort study

P.72 - GDF-15 expression in mitochondrial and other neurological diseases

GDF-15 expression in mitochondrial and other neurological diseases

P.53Potentially confounding variables of mitochondria biomarker GDF-15

A hypomorphic variant in the translocase of the outer mitochondrial membrane complex subunit TOMM7 causes short stature and developmental delay

GDF-15 expression in multiple sclerosis and limbic encephalitis

Mitochondrial tRNA gene mutations in patients having mitochondrial disease with lactic acidosis

Increased mitochondrial processing intermediates associated with three tRNA(Leu(UUR)) gene mutations

Effect of bezafibrate treatment on late-onset mitochondrial myopathy in mice

Growth differentiation factor 15 as a useful biomarker for mitochondrial disorders

mTORC1 Regulates Mitochondrial Integrated Stress Response and Mitochondrial Myopathy Progression

MELAS: A nationwide prospective cohort study of 96 patients in Japan

Advanced Test of Attention in Children with Attention-Deficit/Hyperactivity Disorder in Japan for Evaluation of Methylphenidate and Atomoxetine Effects

Clinical characteristics of cytochrome P450 oxidoreductase deficiency: a nationwide survey in Japan

GDF15 is a novel biomarker to evaluate efficacy of pyruvate therapy for mitochondrial diseases

An exploratory study to identify neonatal arterial ischemic stroke: A single-center study

Laryngotracheal separation surgery in a patient with severe Angelman syndrome involving a 19.3 Mb deletion on 15q11.2–q14

Congenital Hypothyroidism Due to Truncating PAX8 Mutations: A Case Series and Molecular Function Studies

Molecular pathology of MELAS and l-arginine effects

Anorexia Nervosa during Adolescence Is Associated with Decreased Gray Matter Volume in the Inferior Frontal Gyrus

Urinary stone in a 12-year-old adolescent with new-onset type 1 diabetes and diabetic ketoacidosis

Suchergebnisse filtern