Keyphrases
Thymidine Phosphorylase
100%
Molecular Study
100%
Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE)
100%
Biochemical Studies
100%
Egyptian Patients
100%
Enzyme Activity
50%
Early Detection
16%
Therapeutic Potential
16%
Neuropathy
16%
Mitochondrial Disease
16%
Prenatal Diagnosis
16%
Brain Magnetic Resonance Imaging
16%
Direct Sequencing
16%
Autosomal Recessive
16%
Muscle Biopsy
16%
Cachexia
16%
Neurological Examination
16%
Histochemical Analysis
16%
Gene Sequencing
16%
Patient Background
16%
Carrier Screening
16%
Pedigree
16%
Pathogenic mutations
16%
Leukoencephalopathy
16%
Sensory Neural Hearing Loss
16%
Biochemical Detection
16%
Molecular Screening
16%
Heterozygous mutation
16%
Mitochondrial Respiratory Chain Enzymes
16%
Cytochrome c Oxidase
16%
Complex I Deficiency
16%
Mitochondrial Respiratory Chain Complexes
16%
Early State
16%
Gastrointestinal Dysmotility
16%
Enzyme Assay
16%
Biochemical Assay
16%
Histochemical Assay
16%
Diagnostic Delay
16%
New Therapeutics
16%
Homozygous mutation
16%
Molecular Findings
16%
INIS
patients
100%
mitochondria
100%
thymidine
75%
phosphorylases
75%
genes
50%
mutations
50%
enzyme activity
37%
diseases
25%
muscles
25%
chains
25%
testing
12%
screening
12%
detection
12%
nmr imaging
12%
biopsy
12%
risks
12%
symptoms
12%
brain
12%
losses
12%
hearings
12%
enzymes
12%
carriers
12%
oxidases
12%
homogenates
12%
cytochromes
12%
iodine complexes
12%
Medicine and Dentistry
Thymidine Phosphorylase
100%
MNGIE Syndrome
100%
Enzyme Activity
50%
Mitochondrial Neurogastrointestinal Encephalopathy Syndrome
50%
Disease
33%
Respiratory Chain
33%
Magnetic Resonance Imaging
16%
Cachexia
16%
Muscle Biopsy
16%
Diagnostic Delay
16%
Histochemistry
16%
Gastrointestinal Motility Disorder
16%
Cytochrome C Oxidase
16%
Prenatal Diagnosis
16%
Sensorineural Hearing Loss
16%
Neurologic Examination
16%
Disorders of Mitochondrial Functions
16%
Gene Sequence
16%
Pedigree
16%
Autosomal Recessive Disorder
16%
Sensory Neuropathy
16%
Enzyme Assay
16%
Carrier Testing
16%
Complex I Deficiency
16%
Leukoencephalopathy
16%
Biochemistry, Genetics and Molecular Biology
Thymidine Phosphorylase
100%
Enzyme Activity
50%
Mitochondrial Neurogastrointestinal Encephalopathy Syndrome
50%
Electron Transport Chain
33%
Magnetism
16%
Pedigree
16%
Homogenate
16%
Cytochrome C Oxidase
16%
Gene Sequence
16%
Autosomal Recessive Disorder
16%
Mitochondrial Disorder
16%
Enzyme Assay
16%