User:Dpryan
I'm was a grad student at UCSF in the Ptáček lab, where I finished my PhD in neuroscience in March 2010. I've worked primarily on thyrotoxic hypokalemic periodic paralysis (though I'm not touching the article given the COI issues surrounding my position in the field). I am currently a post-doc at the Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE) working on neurocognitive disorders. I'm slowly going through and modifying the ion channel and channelopathy pages since that's what I'm an expert in. I did a little work on the Lima, Ohio page, since I'm from there.
To contact me, click on the "E-mail this user" link on the side bar.
Articles should (more or less) conform to the Medicine manual of style.
To add/work on (page(s) currently in progress are in the Sandbox):
- Various ion channel pages
- Channel kinetics pages
Inherited epilepsy and seizure disorders
GEFS+Severe myoclonic epilepsy of infancyIntractable epilepsy in childhoodChildhood absence epilepsy
...and febrile convulsions
Movement/Developmental Disorders
- Sodium channelopathies:
- Calcium Channelopathies
- Hypokalemic periodic paralysis (CACN1AS)
- Chloride channelopathies
- Myotonia congenita (ClCN1)
- Potassium channelopathies
- Andersen-Tawil syndrome (KCNJ2)
Cardiovascular specific disorders
- Brugada syndrome (NaV1.5)
- Long QT syndrome (NaV1.5, KCNQ1, KCNH2)
- Ventricular fibrillation, idiopathic (NaV1.5)
- Atrial fibrillation (KCNQ1)
- Short QT syndrome(KCNQ1)
- Sick sinus syndrome (HCN4)
Timothy syndrome- Dilated Cardiomyopathy
Vision disorders
Auditory Disorders
- Nonsyndromic deafness (KCNQ4)
Ataxias
Ion/molecule balance
Hypomagnesemia with secondary hypocalcemiaFocal segmental glomerulosclerosisMucolipidosis type IV- Bartter's syndrome (KCNJ1)
- Persistent hyperinsulinemic hypoglycemia of infancy (KCNJ11)
- Diabetes mellitus (KCNJ9, KCNJ11, SUR1)
- Congenital hyperinsulinism/Neonatal diabetes/DEND Syndrome (KCNJ11)
- Congenital hyperinsulinism (SUR1)
Other/unclassified
Pain
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