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Showing 1–10 of 12 results for “Acylation”
Pediatric Neurology · Chapter 47
SECTION 7 Neurometabolic Disorders
acyl-CoA dehydrogenase deficiency and carnitine palmitoyltransferase 2 (CPT-II) deficiency. Glutaric aciduria type 1 is classically associated with widened
Pediatric Neurology · Chapter 47
SECTION 7 Neurometabolic Disorders
acyl-CoA dehydrogenase deficiency and carnitine palmitoyltransferase 2 (CPT-II) deficiency. Glutaric aciduria type 1 is classically associated with widened
Pediatric Neurology · Chapter 47
SECTION 7 Neurometabolic Disorders
acyl-CoA dehydrogenase deficiency and carnitine palmitoyltransferase 2 (CPT-II) deficiency. Glutaric aciduria type 1 is classically associated with widened
Pediatric Neurology · Chapter 51
Case 36 Severe Neonatal Communicating Hydrocephalus
acyl-CoA dehydrogenase deficiency, some mitochondrial disorders (e.g., fumarase deficiency), peroxisomal biogenic disorders (e.g., Zellweger spectrum), and disorders of O-mannosylation
Pediatric Neurology · Chapter 104
Subject Index
acyl-CoA oxidase deficiency, 169 Persistent fetal vasculature (PFV), 250 Petechial hemorrhages, multifocal susceptibility reflecting, 331f Phenotypes, 188 Pilocytic astrocytoma
Pediatric Neurology · Chapter 42
Case 28 A Child Who Drops Very Quickly in His School Performance
acyl-CoA oxidase deficiency: Much rarer with some similar MRI features. The typical findings are progressive white matter abnormalities, atrophy
Pediatric Neurology · Chapter 104
Subject Index
acyl-CoA oxidase deficiency, 169 Persistent fetal vasculature (PFV), 250 Petechial hemorrhages, multifocal susceptibility reflecting, 331f Phenotypes, 188 Pilocytic astrocytoma
Pediatric Neurology · Chapter 42
Case 28 A Child Who Drops Very Quickly in His School Performance
acyl-CoA oxidase deficiency: Much rarer with some similar MRI features. The typical findings are progressive white matter abnormalities, atrophy
Pediatric Neurology · Chapter 104
Subject Index
acyl-CoA oxidase deficiency, 169 Persistent fetal vasculature (PFV), 250 Petechial hemorrhages, multifocal susceptibility reflecting, 331f Phenotypes, 188 Pilocytic astrocytoma
Pediatric Neurology · Chapter 51
Case 36 Severe Neonatal Communicating Hydrocephalus
acyl-CoA dehydrogenase deficiency, some mitochondrial disorders (e.g., fumarase deficiency), peroxisomal biogenic disorders (e.g., Zellweger spectrum), and disorders of O-mannosylation
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