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Leila Scholle (1978-)

Naturwissenschaftlerin

Name	Leila Scholle
Time	1978- (Date of birth and death)
Place	Teheran (Geburtsort) Iran Deutschland
Gender	weiblich
Academic degree	Dr. rer. nat. Dr. rer. medic. habil.
Profession	Naturwissenschaftlerin (characteristic profession)
Variant	Leila Motlagh Scholle Leila Motlagh (früherer Name) Leila Scholle
Related	Martin-Luther-Universität Halle-Wittenberg (Habilitation) (2022) Kliniken Halle (Saale)
Source	Homepage: https://www.researchgate.net/profile/Leila_Scholle (Stand: 09.04.2018)
Record type	Person
GND-Identifier	1155731212
Record ID	1155731212
Involved in show all Quantitative whole-body muscle MRI in idiopathic inflammatory myopathies including polymyositis with mitochondrial pathology: indications for a disease spectrum Correlation of Immunomodulatory Cytokines with Tumor Volume and Cerebrospinal Fluid in Vestibular Schwannoma Patients Biochemische Charakterisierung mitochondrialer Myopathien in Trägern der m.3243A>G Mutation und Patienten mit Carnitin-Palmitoyltransferase II-Mangel : kumulative Schrift Camptocormia as a novel phenotype in a heterozygous POLG2 mutation Myalgia in 30 Patients with Suspected Myopathy Palmitate but not oleate exerts a negative effect on oxygen utilization in myoblasts of patients with the m.3243A>G mutation: a pilot study The m.9143T>C variant: recurrent infections and immunodeficiency as an extension of the phenotypic spectrum in MT-ATP6 mutations? Lack of activation of the S113L variant of carnitine palmitoyltransfersase II by cardiolipin

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Leila Scholle (1978-)

Quantitative whole-body muscle MRI in idiopathic inflammatory myopathies including polymyositis with mitochondrial pathology: indications for a disease spectrum

Correlation of Immunomodulatory Cytokines with Tumor Volume and Cerebrospinal Fluid in Vestibular Schwannoma Patients

Biochemische Charakterisierung mitochondrialer Myopathien in Trägern der m.3243A>G Mutation und Patienten mit Carnitin-Palmitoyltransferase II-Mangel : kumulative Schrift

Camptocormia as a novel phenotype in a heterozygous POLG2 mutation

Myalgia in 30 Patients with Suspected Myopathy

Palmitate but not oleate exerts a negative effect on oxygen utilization in myoblasts of patients with the m.3243A>G mutation: a pilot study

The m.9143T>C variant: recurrent infections and immunodeficiency as an extension of the phenotypic spectrum in MT-ATP6 mutations?

Lack of activation of the S113L variant of carnitine palmitoyltransfersase II by cardiolipin