Search Results 611-620 of 16502 for Chiari malformation
The purpose of this study is to characterize the phenotype of SCN1A-positive Dravet Syndrome in subjects aged 6 to 60 months, inclusive. Participation ...
... Chiari malformation, Trigeminal neuralgia, Hydrocephalus, Hyperhidrosis, Brain tumor-associated epilepsy. Show more areas of focus for Sanjeet S. Grewal ...
Some short-term studies in adults with growth hormone deficiency also show that they benefit lean body mass and also muscle tone. Another big endocrine disorder ...
The Upper Limb Reconstruction in UMN Syndrome Clinic offers nonsurgical and surgical care for shoulder, elbow, wrist, and hand dysfunction or deformity.
Zebrafish models of human hearing loss and gene discovery. Usher syndrome type 1 is a condition in which children are born deaf and then begin to lose their ...
Ebstein anomaly (EA) is a rare, complex and highly variable congenital heart malformation characterized by tricuspid valve regurgitation, right ventricle ...
Dravet syndrome is a rare but severe epilepsy syndrome that begins in the first 18 months of life with recurrent and prolonged seizures often triggered by fever ...
... syndrome or congenital malformations at the Mayo Clinic. Additionally, to perform RNA Sequencing and targeted metabolomics analysis to identify alterations ...
... malformations, cavernous malformations, dural arteriovenous fistulas, moyamoya disease, intracranial aneurysms and genetic causes of stroke. The ...
Todd and Karen Wanek Family Program for Hypoplastic Left Heart Syndrome (HLHS). Sections. Overview; About About. About Hypoplastic Left Heart Syndrome (HLHS) ...
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