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User:Dpryan

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606: 650: 530: 702: 733: 28:(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 fĂĽr Neurodegenerative Erkrankungen (DZNE) working on neurocognitive disorders. I'm slowly going through and modifying the 780: 775: 47: 421: 133: 77: 504: 321: 395: 629: 623: 562: 785: 260: 114: 84: 402: 91: 497: 356: 162: 618: 377: 195: 370: 167: 25: 790: 511: 121: 447: 433: 98: 465: 229: 33: 605: 472: 291: 173: 179: 537: 409: 338: 415: 678: 307: 441: 278: 266: 54: 212: 437: 427: 272: 713: 285: 254: 248: 490: 363: 649: 769: 314: 125: 529: 683: 613: 24:, where I finished my PhD in neuroscience in March 2010. I've worked primarily on 751: 29: 37: 701: 732: 741: 137: 43:
To contact me, click on the "E-mail this user" link on the side bar.
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pages since that's what I'm an expert in. I did a little work on the
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Wikipedians by alma mater: University of California, San Francisco
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To add/work on (page(s) currently in progress are in the
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Persistent hyperinsulinemic hypoglycemia of infancy
134:Autosomal dominant nocturnal frontal lobe epilepsy 776:Wikipedians by alma mater: University of Chicago 505:Channelopathy-associated insensitivity to pain 322:X-linked congenital stationary night blindness 46:Articles should (more or less) conform to the 8: 396:Hypomagnesemia with secondary hypocalcemia 26:thyrotoxic hypokalemic periodic paralysis 69:Inherited epilepsy and seizure disorders 7: 696: 670: 644: 600: 552: 524: 261:Ventricular fibrillation, idiopathic 115:Benign familial neonatal convulsions 85:Severe myoclonic epilepsy of infancy 535:This user attends or attended the 403:Focal segmental glomerulosclerosis 14: 559:This user attends or attended the 241:Cardiovascular specific disorders 92:Intractable epilepsy in childhood 731: 726: 700: 648: 604: 578: 528: 498:Paroxysmal extreme pain disorder 148:Movement/Developmental Disorders 357:Episodic and progressive ataxia 163:Hyperkalemic periodic paralysis 378:Spinocerebellar ataxia type-13 196:Hypokalemic periodic paralysis 1: 371:Spinocerebellar ataxia type-6 168:Potassium-aggravated myotonia 786:Wikipedians with PhD degrees 512:Familial hemiplegic migraine 40:page, since I'm from there. 122:Juvenile myoclonic epilepsy 807: 448:Congenital hyperinsulinism 434:Congenital hyperinsulinism 107:...and febrile convulsions 99:Childhood absence epilepsy 16:I'm was a grad student at 707:This user has published 564:University of California, 466:Polycystic kidney disease 222:Potassium channelopathies 61:Various ion channel pages 205:Chloride channelopathies 48:Medicine manual of style 230:Andersen-Tawil syndrome 188:Calcium Channelopathies 155:Sodium channelopathies: 739:God made this user an 473:Malignant hyperthermia 292:Dilated Cardiomyopathy 257:(NaV1.5, KCNQ1, KCNH2) 174:Paramyotonia congenita 64:Channel kinetics pages 539:University of Chicago 430:(KCNJ9, KCNJ11, SUR1) 410:Mucolipidosis type IV 339:Nonsyndromic deafness 679:Doctor of Philosophy 611:This user supported 387:Ion/molecule balance 308:Retinitis pigmentosa 791:Atheist Wikipedians 279:Sick sinus syndrome 267:Atrial fibrillation 180:Myasthenic syndrome 457:Other/unclassified 416:Bartter's syndrome 331:Auditory Disorders 213:Myotonia congenita 764: 763: 759: 758: 721: 720: 714:academic journals 691: 690: 665: 664: 637: 636: 595: 594: 573: 572: 547: 546: 438:Neonatal diabetes 428:Diabetes mellitus 273:Short QT syndrome 798: 735: 727: 710: 704: 697: 677:This user has a 671: 652: 645: 608: 601: 585:This user has a 579: 567: 553: 540: 532: 525: 520: 519: 300:Vision disorders 286:Timothy syndrome 255:Long QT syndrome 249:Brugada syndrome 806: 805: 801: 800: 799: 797: 796: 795: 766: 765: 760: 722: 708: 692: 666: 655:This user runs 638: 596: 574: 565: 563: 560: 548: 538: 514: 507: 500: 493: 491:Erythromelalgia 484: 475: 468: 459: 412: 405: 398: 389: 380: 373: 366: 364:Episodic Ataxia 359: 350: 333: 324: 317: 302: 288: 243: 176: 150: 141: 129: 117: 108: 101: 94: 87: 80: 71: 12: 11: 5: 804: 802: 794: 793: 788: 783: 778: 768: 767: 762: 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Do 450:(SUR1) 281:(HCN4) 138:ADNFLE 658:macOS 78:GEFS+ 630:2012 627:and 624:2008 617:for 582:Web 556:UCSF 482:Pain 32:and 18:UCSF 747:you 674:PhD 621:in 57:): 772:: 755:? 591:. 50:. 717:. 687:. 661:. 633:. 543:. 440:/ 436:/ 140:) 136:( 128:) 124:(

Index

UCSF
Ptáček lab
thyrotoxic hypokalemic periodic paralysis
ion channel
channelopathy
Lima, Ohio
Medicine manual of style
Sandbox
GEFS+
Severe myoclonic epilepsy of infancy
Intractable epilepsy in childhood
Childhood absence epilepsy
Benign familial neonatal convulsions
Juvenile myoclonic epilepsy
Janz syndrome
Autosomal dominant nocturnal frontal lobe epilepsy
ADNFLE
Hyperkalemic periodic paralysis
Potassium-aggravated myotonia
Paramyotonia congenita
Myasthenic syndrome
Hypokalemic periodic paralysis
Myotonia congenita
Andersen-Tawil syndrome
Brugada syndrome
Long QT syndrome
Ventricular fibrillation, idiopathic
Atrial fibrillation
Short QT syndrome
Sick sinus syndrome

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