User:Dpryan
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I'm a grad student at UCSF in the Ptáček lab. I'm slowly going through and modifying the ion channel and channelopathy pages since that's what I'm an expert in. I'm 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:
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GEFS+Severe myoclonic epilepsy of infancyIntractable epilepsy in childhoodChildhood absence epilepsy
...and febrile convulsions
- Movement/Developmental Disorders:
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- Sodium channelopathies:
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- Hyperkalemic periodic paralysis
- Potassium-aggravated myotonias
- Sodium channel myotonias
- Periodica paralytica paramyotonia
Paramyotonia congenita- Myasthenic syndrome
- Calcium Channelopathies
- Chloride channelopathies
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- Myotonia congenita (ClCN1)
- Potassium channelopathies
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- Periodic paralysis (KCNC4)
- Andersen-Tawil syndrome (KCNJ2)
- Cardiovascular specific disorders:
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- Brugada syndrome (NaV1.5)
- Inherited erythromelalgia (NaV1.7)
- Long QT syndrome (NaV1.5, KCNQ1, KCNH2)
- Ventricular fibrillation, idiopathic (NaV1.5)
- Atrial fibrillation (KCNQ1)
- Short QT syndrome(KCNQ1)
- Sick sinus syndrome (HCN4)
- Vision disorders:
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- Retinitis pigmentosa (CNGA1, CNGB1)
- Achromatopsia (CNGA3, CNGB3)
- X-linked congenital stationary night blindness type 2 (CACNA1F)
- Auditory Disorders:
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- Nonsyndromic deafness (KCNQ4)
- Ataxias:
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episodic and progressive ataxia- Episodic Ataxia Type-1/myokymia (KCNA1)
- Episodic ataxia type 2 (CACNA1A)
Spinocerebellar ataxia type-6
- Ion/molecule balance
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Hypomagnesemia with secondary hypocalcemia- Bartter's syndrome (KCNJ1)
- Persistent hyperinsulinemic hypoglycemia of infancy (KCNJ11)
- Diabetes mellitus? (KCNJ9, KCNJ11, SUR1)
- Other/unclassified:
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- Beckwith-Wiedemann_syndrome (KCNQ1)
- Malignant hyperthermia (CACN1AS)
Familial hemiplegic migraine
