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La ricerca find articoli where authors phrase all words 'Nance, MA' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 36 riferimenti
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    1. Nance, MA; Myers, RH
      Juvenile onset Huntington's disease - Clinical and research perspectives

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    2. Scott, WK; Nance, MA; Watts, RL; Hubble, JP; Koller, WC; Lyons, K; Pahwa, R; Stern, MB; Colcher, A; Hiner, BC; Jankovic, J; Ondo, WG; Allen, FH; Goetz, CG; Small, GW; Masterman, D; Mastaglia, F; Laing, NG; Stajich, JM; Slotterbeck, B; Booze, MW; Ribble, RC; Rampersaud, E; West, SG; Gibson, RA; Middleton, LT; Roses, AD; Haines, JL; Scott, BL; Vance, JM; Pericak-Vance, MA
      Complete genomic screen in parkinson disease - Evidence for multiple genes

      JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
    3. Martin, ER; Scott, WK; Nance, MA; Watts, RL; Hubble, JP; Koller, WC; Lyons, K; Pahwa, R; Stern, MB; Colcher, A; Hiner, BC; Jankovic, J; Ondo, WG; Allen, FH; Goetz, CG; Small, GW; Masterman, D; Mastaglia, F; Laing, NG; Stajich, JM; Ribble, RC; Booze, MW; Rogala, A; Hauser, MA; Zhang, FY; Gibson, RA; Middleton, LT; Roses, AD; Haines, JL; Scott, BL; Pericak-Vance, MA; Vance, JM
      Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease

      JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
    4. Svenson, IK; Ashley-Koch, AE; Gaskell, PC; Riney, TJ; Cumming, WJK; Kingston, HM; Hogan, EL; Boustany, RMN; Vance, JM; Nance, MA; Pericak-Vance, MA; Marchuk, DA
      Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia

      AMERICAN JOURNAL OF HUMAN GENETICS
    5. Potter, NT; Nance, MA
      Genetic testing for ataxia in North America

      MOLECULAR DIAGNOSIS
    6. Nance, MA; Nuttall, FQ; Econs, MJ; Lyles, KW; Viles, KD; Vance, JM; Pericak-Vance, MA; Speer, MC
      Heterogeneity in Paget disease of the bone

      AMERICAN JOURNAL OF MEDICAL GENETICS
    7. Anderson, JL; Khan, M; David, WS; Mahdavi, Z; Nuttall, FQ; Krech, E; West, SG; Vance, JM; Pericak-Vance, MA; Nance, MA
      Confirmation of linkage of hereditary partial lipodystrophy to chromosome 1q21-22

      AMERICAN JOURNAL OF MEDICAL GENETICS
    8. Nance, MA; Mathias-Hagen, V; Breningstall, G; Wick, MJ; McGlennen, RC
      Analysis of a very large trinucleotide repeat in a patient with juvenile Huntington's disease

      NEUROLOGY
    9. Nance, MA
      Huntington disease: Clinical, genetic, and social aspects

      JOURNAL OF GERIATRIC PSYCHIATRY AND NEUROLOGY
    10. NANCE MA
      LACK OF COUNSELING WHEN PREDICTIVE TESTS FOR HUNTINGTONS DISEASES AREPERFORMED OUTSIDE OF PREDICTIVE TESTING CENTERS

      Neurology
    11. NANCE MA; RAABE WA; MIDANI H; KOLODNY EH; DAVID WS; MEGNA L; PERICAKVANCE MA; HAINES JL
      CLINICAL HETEROGENEITY OF FAMILIAL SPASTIC PARAPLEGIA LINKED TO CHROMOSOME 2P21

      Human heredity
    12. NANCE MA; SELTZER W; ASHIZAWA T; BENNETT R; MCINTOSH N; MYERS RH; POTTER T; SHEA DK
      LABORATORY GUIDELINES FOR HUNTINGTON-DISEASE GENETIC TESTING

      American journal of human genetics
    13. NANCE MA
      CLINICAL ASPECTS OF CAG REPEAT DISEASES

      Brain pathology
    14. NANCE MA; ABRAMSON R; ASHIZAWA T; CODORI AM; FOX M; GETTIG B; MYERS RH; QUAID K; SELTZER W; SHEA DK; WEXLER N; ZANKO A; PROUD V; RICHTER S; HAUCK L; BROOME D; BASS H; JONES OW; ZANKO A; BODELL A; TAYLOR L; HAVERKAMP C; HEIMLER A; DIMAIO M; HAUN R; DIAMOND T; JONES R; YIM D; DONLON S; EVERS C; SHANNON K; LEBEL R; POLZIN S; MILLER J; QUAID K; GRAY C; GODFREY N; MYERS R; UHLMANN W; LUDOWESE C; LEROY B; OTTO E; JOHNSON J; MCCORMACK M; COPE J; PALLADINO L; LEWIS J; MCKENNA C; HICKEY C; THOMSON L; WATERSON J; HUELSMAN K; LINARD S; SCHAEFER F; RUBENSTEIN J; KOVAK K; GOODWIN D; GODMILOW L; SCHRAMKE C; SKOREYSOLLBERG P; POTTER N; HANNIG V; BROOKSHIRE G; HELLER K; KESTER M; LEONARD K; MENGDEN GA; BATY B; ALLINSON P; BENNETT R; HINER B; GOONEWARDENA P; SPECTOR E; MCINTOSH N; MUELLER OT; SHOFFNER J; BERRYKRAVIS E; DEMARCHI J; KASCH L; MATTHIASHAGEN V; BARTHOLOMEW D; PRIOR T; SCHAEFER F; GOODWIN D; VNENCAKJONES C; POTTER N; RICHARDS S
      GENETIC TESTING OF CHILDREN AT RISK FOR HUNTINGTONS-DISEASE

      Neurology
    15. NANCE MA
      NEUROGENETICS AND PRIMARY-CARE

      Neurology
    16. NANCE MA
      VOLUNTARY MONITORING OF PREDICTIVE TESTING PROGRAMS FOR HUNTINGTON-DISEASE - THE UNITED-STATES HUNTINGTON-DISEASE GENETIC TESTING GROUP (USHD GTG)

      American journal of human genetics
    17. SEQUEIROS J; NANCE MA
      OFFER AND UTILIZATION OF GENETIC TESTING IN THE DOMINANT ATAXIAS - TOWARDS GUIDELINES

      American journal of human genetics
    18. VISINTAINER CL; NANCE MA
      ANONYMOUS PREDICTIVE TESTING FOR HUNTINGTON-DISEASE IN THE UNITED-STATES

      American journal of human genetics
    19. NANCE MA; SANDERS G
      CHARACTERISTICS OF INDIVIDUALS WITH HUNTINGTON DISEASE IN LONG-TERM-CARE

      Movement disorders
    20. NANCE MA; WESTPHAL B; NUGENT S
      DIAGNOSIS OF PATIENTS PRESENTING TO A HUNTINGTON DISEASE (HD) CLINIC WITHOUT A FAMILY HISTORY OF HD

      Neurology
    21. NANCE MA; BOYADJIEV S; PRATT VM; TAYLOR S; HODES ME; DLOUHY SR
      ADULT-ONSET NEURODEGENERATIVE DISORDER DUE TO PROTEOLIPID PROTEIN GENE MUTATION IN THE MOTHER OF A MAN WITH PELIZAEUS-MERZBACHER DISEASE

      Neurology
    22. DAVIS PH; CLARKE WR; BENDIXEN BH; ADAMS HP; WOOLSON RF; CULEBRAS A; JACOBY MR; GOMEZ FJ; HUGHES B; DYKEN ME; UC EY; WOJCIESZEK JM; KAPPELLE LJ; TANNA AB; MITCHELL VL; KING MK; BRUNO A; LAKIND ED; JEFFREY DR; MLADINICH EK; IQBAL J; REINERS M; BARRETT DW; SHIBUYA D; WILLIAMS JK; RUSSELL P; CHAPIN JE; AHMED W; CARTER S; JEFFRIES L; KARANJIA PM; MADDEN KP; RUGGLES KH; MICKEL SF; GOTTSCHALK PG; HANSOTIA PL; SORENSON RW; JACOBSON DM; HINER BC; MANCL K; LUKASIK E; BURCH CM; GOMEZ CR; MALKOFF MD; TULYAPRONCHOTE R; SAUER CM; RIAZ G; SCHMIDT JG; MALIK MM; VIVESCASTRO LR; CRUZFLORES S; THOMPSON DW; BANET GA; JACKSON CM; ROTHROCK JF; LYDEN PD; BRODY ML; ZWEIFLER RM; TOM T; FORDE G; KELLY NM; HELGASON CM; HIER DB; SHAPIRO RA; BRINT SU; GNUTEK T; HOFF J; OCONNELL D; FISHER MJ; AMERISO SF; GARABEDIAN MH; MACKO RF; HANNA M; YEGYAN GA; PARK SJU; MARTIN A; SCICLI A; LIBMAN RB; KWIATKOWSKI TG; KANNER RM; WIRKOWSKI EJ; ABRAMS R; DONNARUMA R; CULLEN V; ROSENBAUM DM; SPARR SA; KATZ PM; VALENCIA AM; KLONOWSKI E; GORDON DL; THIEL AA; FREDERICKS RK; SINGH R; RAFIQUE A; DENDINGER J; GORELICK PB; RISKIN BJ; MIRZA DB; KELLY MA; BIJARI A; MURRAY JC; CURTIN J; BOZZOLA FG; KOFMAN JC; PAJEAU AK; SHANMUGAM V; AGNELLODIMITRIJEVIC W; BROWN N; DOLLEAR WC; WEINBERGER JM; TUHRIM S; RUDOLPH SH; HOROWITZ DR; SHEINART KF; GONDOLO TM; ALI J; BITTON A; FELDMANN E; WILTERDINK JL; FURIE K; BALDWIN E; RICKS L; CAREY GC; MARTIR NM; KENT PF; RABIEE H; GUEVARA RA; BANGCO MS; SHAH K; ATTARIAN H; PASTOR D; FICARRA C; MOHR JP; SACCO RL; CLAVIJO M; BILLER J; SAVER JL; FRANK JI; PATRICK JT; FERNANDEZBEER E; BYER JA; WHITE HH; SUNDRANI S; ZAFAR MJ; ARORA R; GAMBOA EC; STACY M; BONNETT A; KELLEY C; COULL BM; BRILEY DP; CLARK WM; KENNY C; AUSTIN T; DEGARMO PL; ANDERSON DC; TARREL RM; NANCE MA; BUNDLIE SR; DOYLE JJ; DIERICH M; LOVE BB; STRUCK LK; MUELLER C; HOGAN EL; CARTER TD; GURECKI P; PLYER JW; MUNTZPOPE BK; HOLLANDER J; HONCH GW; LESSER HD; WEBER C; WROBEL CJ; LERAMO OB; BUXTON S; FAYAD PB; BRASS LM; PAVALKIS FJ; DUROCHER A; PASCUZZI RM; POURMAND R; REDDY VR; CHADWICK LR; WARACH SJ; MAYMAN CI; DARBY DG; DASHE JF; TIJERINA ML; MANDELBAUM MA; HASSAN RU; ABBAS DH; OLMSTEAD CG; SEDLACEK L; MILLER AE; KEILSON MJ; BRUINING KM; DREXLER EE; MORGANTE L; RAMIREZLASSEPAS M; TULLOCH JW; QUINONES MR; CLAVEL A; MENDEZ MF; ZHANG S; ALA TA; ESPINOSA C; JOHNSTON KL; HWANG TL; BRANNON WL; TRUJILLANO AC; FRANK RL; KASE CS; WOLF PA; BABIKIAN VL; LICATAGEHR EE; ALLEN NC; CHATURVEDI S; CHAPPIDI PV; TVARDEK L; HOMER D; NEELY S; CARPENTER J; FUTRELL NN; WANG D; DAVIS KA; KORSNACK AM; BASSAM BA; CUNNINGHAM S; DRINKARD R; SAVER JL; STARKMAN S; HOROWITZ SH; LAVA NS; MANNING M; LOVE BB; GRIMSMAN KJ; OLSON JD; PENNELL BJ; JOHNSON K; CORNELL SH; CROSBY DL; SIMONSON TM; KRUMBHOLZ V; COMINE JA; ZALESKY CR; WASEK PA; DIELEMAN JA; PAULSEN JM; BOREEN JP; JONES MF; ROBB BM; OBERBROECKLING LA; HANSEN MD; HICKLIN KM; FRANKOWSKI RF; GREENBERG CS; HARKER LA; WHISNANT JP; FINCHAM RW; KISKER TC; WALLACE RB
      SILENT CEREBRAL INFARCTION IN PATIENTS ENROLLED IN THE TOAST STUDY

      Neurology
    23. NANCE MA; WESTPHAL B
      DIAGNOSIS OF PATIENTS PRESENTING TO A HUNTINGTONS-DISEASE CLINIC WITHOUT A FAMILY HISTORY OF HUNTINGTONS-DISEASE

      Neurology
    24. MIDANI H; NANCE MA; PARRY G
      X-LINKED CHARCOT-MARIE-TOOTH DISEASE - AN INHERITED AXONAL NEUROPATHY

      Neurology
    25. CHESEBRO JH; WIEBERS DO; HOLLAND AE; BARDSLEY WT; LITIN SC; MEISSNER I; ZERBE DM; FLAKER GC; WEBEL R; NOLTE B; STEVENSON P; BYER J; WRIGHT W; ANDERSON DC; ASINGER RW; NEWBURG SM; BUNDLIE SR; FARMER CC; KOLLER RL; HAUGLAND JM; NANCE MA; TARREL RM; DUNBAR DN; JORGENSEN CR; SHARKEY SW; LEONARD AD; KANTER MC; SOLOMON DH; ZABALGOITIA M; MCANULTY JH; MARCHANT C; COULL BM; KELLEY RE; CHAHINE R; PALERMO M; TEIXEIRO P; FELDMAN G; HAYWARD A; MACMILLAN K; GANDARA E; ANDERSON W; BLANK N; STRAUSS R; FEINBERG WM; VOLD BK; KERN KB; APPLETON C; BRUCK D; DORR S; DITTRICH HC; ROTHROCK JF; HAGENHOFF C; LOGAN WR; HAMILTON WP; GREEN BJ; BACON RS; HELGASON CM; KONDOS GT; HOFF J; HALPERIN JL; ROTHLAUF EB; WEINBERGER JM; GOLDMAN ME; MILLER VT; HOCKERSMITH CJ; COHEN BA; JANOSIK DL; CADELL DJ; KELLERMAN L; GOMEZ CR; LABOVITZ AJ; ROTHBART RM; BAILEY GH; BURKHARDT C; HORWITZ L; BLACKSHEAR JL; WEAVER L; BAKER V; LEE G; LANE G; RUBINO F; SAFFORD R; KRONMAL RA; MCBRIDE R; PEARCE L; FLETCHER KA; NASCO E; HART RG; SHERMAN DG; TALBERT RL; HEBERLING PA; COLTON T; LEVY DE; MARSH JD; WELCH KMA; MARLER JR; WALKER MD
      BLEEDING DURING ANTITHROMBOTIC THERAPY IN PATIENTS WITH ATRIAL-FIBRILLATION

      Archives of internal medicine
    26. NANCE MA
      HUNTINGTON DISEASE - ANOTHER CHAPTER REWRITTEN

      American journal of human genetics
    27. LUDOWESE CJ; NANCE MA
      GROUP-COUNSELING FOR NEW HUNTINGTON DISEASE FAMILIES

      American journal of human genetics
    28. NANCE MA; RAABE WA; MIDANI H; DAVID WS; MEGNA L; PERICAKVANCE MA; HAINES JL
      CONFIRMATION LINKAGE OF FAMILIAL SPASTIC PARAPARESIS TO CHROMOSOME 2P21

      American journal of human genetics
    29. HAGEN VLM; NANCE MA; PARKER TL; LUDOWESE CJ; ALLINSON PS; KELLY TE; LEROY BS; ORR HT; MCGLENNEN RC
      HUNTINGTON DISEASE INTERMEDIATE ALLELES - THE UNIVERSITY-OF-MINNESOTAEXPERIENCE WITH HUNTINGTIN GENE MUTATION TESTING

      American journal of human genetics
    30. PARKER TL; NANCE MA; HAGEN VLM; BRENINGSTALL G; MCGLENNEN RC
      VERY HIGH CAG REPEAT NUMBER IN HUNTINGTON DISEASE

      American journal of human genetics
    31. NANCE MA; SEVENICH EA; SCHUT LJ
      KNOWLEDGE OF GENETICS AND ATTITUDES TOWARD GENETIC TESTING IN 2 HEREDITARY ATAXIA (SCA-1) KINDREDS

      American journal of medical genetics
    32. NANCE MA; LUDOWESE CJ
      DIAGNOSIS OF HUNTINGTON-DISEASE - MODEL FOR A PREDICTIVE TESTING PROGRAM BASED ON UNDERSTANDING THE STAGES OF PSYCHOLOGICAL RESPONSE

      American journal of medical genetics
    33. MCBRIDE R; CHESEBRO JH; WIEBERS DO; HOLLAND AE; LINKER S; BARDSLEY WT; KOPECKY S; LITIN SC; MEISSNER I; ZERBE DM; FLAKER GC; WEBEL R; NOLTE B; STEVENSON P; BYER J; JENKINS JS; WRIGHT W; ANDERSON DC; ASINGER RW; NEWBURG SM; BUNDLIE SR; FARMER CC; KOLLER RL; HAUGLAND JM; NANCE MA; TARREL RM; DUNBAR DN; JORGENSEN CR; SHARKEY SW; LEONARD ADS; KANTER MC; SOLOMON DH; ZABALGOITIA M; MCANULTY JH; MARCHANT C; COULL BM; KELLEY RE; CHAHINE R; PALERMO M; TEIXEIRO P; FELDMAN G; HAYWARD A; MACMILLAN K; GANDARA E; ANDERSON W; BLANK N; STRAUSS R; FEINBERG WM; VOLD BK; KERN KB; APPLETON C; BRUCK D; DORR S; DITTRICH HC; ROTHROCK JF; KERRIDGE C; LOGAN WR; HAMILTON WP; GREEN BJ; BACON RS; HELGASON CM; KONDOS GT; HOFF J; MCRAE RP; HALPERIN JL; ROTHLAUF EB; WEINBERGER JM; GOLDMAN ME; MILLER VT; HOCKERSMITH CJ; COHEN BA; JANOSIK DL; CADELL DJ; KELLERMAN L; GOMEZ CR; LABOVITZ AJ; ROTHBART RM; BAILEY GH; BURKHARDT C; HORWITZ L; BLACKSHEAR JL; WEAVER L; BAKER V; LEE G; LANE G; RUBINO F; SAFFORD R; KRONMAL RA; PEARCE LA; FLETCHER KA; NASCO E; HART RG; SHERMAN DG; TALBERT RL; DACY TL; HERBERLING PA
      WARFARIN VERSUS ASPIRIN FOR PREVENTION OF THROMBOEMBOLISM IN ATRIAL-FIBRILLATION - STROKE PREVENTION IN ATRIAL-FIBRILLATION-II STUDY

      Lancet
    34. ALBANESE MA; CLARKE WR; ADAMS HP; WOOLSON RF; BENDIXEN BH; DAVIS PH; JACOBY MR; GOMEZ FJ; DYKEN ME; UC EY; WOJCIESZEK JM; KAPPELLE LJ; TANNA AB; MITCHELL VL; GOMEZ CR; MALKOFF MD; TULYAPRONCHOTE R; SAUER CM; RIAZ G; SCHMIDT JG; MALIK MM; BANET GA; KARANJIA PN; MADDEN KP; RUGGLES KH; MICKEL SF; GOTTSCHALK PG; HANSOTIA PL; SORENSON RW; JACOBSON DM; HINER BC; MANCL K; LUKASIK E; BRUNO A; LAKIND ED; JEFFREY DR; MLADINICH EK; IQBAL J; REINERS M; BARRETT DW; SHIBUYA D; WILLIAMS JK; RUSSELL P; KING MK; CHAPIN JE; CARTER S; JEFFRIES L; HIER DB; SHAPIRO RA; BRINT SU; HOFF J; OCONNELL D; FISHER MJ; AMERISO SF; GARABEDIAN MH; MACKO RF; HANNA M; YEGYAN GA; MARTIN A; SCICLI A; JACKSON CM; ROTHROCK JF; LYDEN PD; BRODY ML; ZWEIFLER RM; KELLY NM; GORDON DL; THIEL AA; FREDERICKS RK; SINGH R; DENDINGER J; GORELICK PB; RISKIN BJ; MIRZA DB; KELLY MA; BIJARI A; MURRAY JC; CURTIN J; BOZZOLA FG; KOFMAN JC; BROWN N; DOLLEAR WC; WEINBERGER JM; TUHRIM S; RUDOLPH SH; HOROWITZ DR; SHEINART KF; GONDOLO TM; ALI J; BITTON A; BILLER J; SAVER JL; FRANK JI; PATRICK JT; FERNANDEZBEER E; CHADWICK L; FELDMANN E; WILTERDINK JL; RICKS L; MOHR JP; SACCO RL; CLAVIJO M; ROSENBAUM DM; SPARR SA; KATZ PM; KLONOWSKI E; BYER JA; WHITE HH; SUNDRANI S; ZAFAR MJ; ARORA R; GAMBOA EC; STACY M; BONNETT A; KELLEY C; CULEBRAS A; CAREY GC; MARTIR NM; KENT PF; RABIEE H; GUEVARA RA; BANGCO MS; PASTOR D; FICARRA C; COULL BM; BRILEY DP; CLARK WM; KENNY C; AUSTIN T; DEGARMO PL; ANDERSON DC; TARREL RM; NANCE MA; BUNDLIE SR; DOYLE JJ; DIERICH M; LOVE BB; STRUCK LK; MUELLER C; HOGAN EL; CARTER TD; GURECKI P; PLYER JW; MUNTZPOPE BK; LIBMAN RB; KWIATKOWSKI TG; KANNER RM; DONNARUMA R; CULLEN V; FAYAD PB; BRASS LM; PAVALKIS FJ; WROBEL CJ; LERAMO OB; BUXTON S; HOLLANDER J; HONCH GW; WEBER C; MAYMAN CI; WARACH SJ; TIJERINA ML; MANDELBAUM MA; HASSAN RU; ABBAS DH; OLMSTEAD CG; SEDLACEK L; MILLER AE; KEILSON MJ; BRUINING KM; DREXLER EE; MORGANTE L; RAMIREZLASSEPAS M; TULLOCH JW; QUINONES MR; CLAVEL A; MENDEZ MF; ZHANG S; ALA TA; ESPINOSA C; JOHNSTON KL; KASE CS; WOLF PA; BABIKIAN VL; LICATAGEHR EE; ALLEN NC; HOMER D; NEELY S; CARPENTER J; HOROWITZ SH; LAVA NS; MANNING M; GRIMSMAN KJ; OLSON JD; PENNELL BJ; JOHNSON K; CORNELL SH; CROSBY DL; SIMPSON TM; KRUMBHOLZ V; ZALESKY CR; WASEK PA; DIELEMAN JA; PAULSEN JM; BOREEN JP; JONES MF; ROBB BM; OBERBROECKLING LA; HANSEN MD; HICKLIN KM; DYKEN ML; FRANKOWSKI RF; GREENBERG CS; HARKER LA; WHISNANT JP; FINCHAM RW; KISKER TC; WALLACE RB; DAY HJ; DETRE KM; GROTTA JC; HALEY EC; LONGSTRETH WT; MARLER JR
      ENSURING RELIABILITY OF OUTCOME MEASURES IN MULTICENTER CLINICAL-TRIALS OF TREATMENTS FOR ACUTE ISCHEMIC STROKE - THE PROGRAM DEVELOPED FORTHE TRIAL OF ORG-10172 IN ACUTE STROKE TREATMENT (TOAST)

      Stroke
    35. GORDON DL; BENDIXEN BH; ADAMS HP; CLARKE W; KAPPELLE LJ; WOOLSON RF; KASE CS; WOLF PA; BABIKIAN VL; LICATAGEHR EE; ALLEN N; BRASS LM; FAYAD PB; PAVALKIS FJ; WEINBERGER JM; TUHRIM S; RUDOLPH SH; HOROWITZ DR; BITTON A; MOHR JP; SACCO RL; CLAVIJO M; ROSENBAUM DM; SPARR SA; KATZ P; KLONOWSKI E; CULEBRAS A; CAREY G; MARTIR NI; FICARRA C; HOGAN EL; CARTER T; GURECKI P; MUNTZ BK; RAMIREZLASSEPAS M; TULLOCH JW; QUINONES MR; MENDEZ M; ZHANG SM; ALA T; JOHNSTON KC; ANDERSON DC; TARREL RM; NANCE MA; BUNDLIE SR; DIERICH M; HELGASON CM; HIER DB; SHAPIRO RA; BRINT S; HOFF J; KARANJIA PN; MADDEN KP; RUGGLES KH; MICKEL SF; GOTTSCHALK PG; HANSOTIA PI; SORENSON RW; JACOBSON DM; HINER BC; MANCL K; GORELICK PB; RISKIN B; MIRZA D; KELLY M; BIJARI A; KOFMAN J; DOLLEAR WC; GOMEZ CR; MALKOFF MD; RIAZ G; SCHMIDT JG; MALIK MM; BANET G; BYER JA; GAMBOA E; STACY M; BONNETT A; FELDMANN E; WILTERDINK JL; RICKS L; BRUNO A; LAKIND E; JEFFREY DR; MLANDINICH EK; KING M; CHAPIN JE; CARTER S; FISHER M; AMERISO S; MACKO RF; MARTIN A; ROTHROCK JF; LYDEN PD; BRODY ML; KELLY NM; LOVE BB; COULL BM; STRUCK LK; BRILEY DP; DENDINGER J; CLARK WM; AUSTIN T; MUELLER C; DEGARMO PL; ADAMS HP; DYKEN E; UC EY; BENDIXEN B; WOJCIESZEK J; KAPPELLE J; MITCHELL V; BILLER J; FRANK J; SAVER JJ; CHADWICK L; MAYMAN CI; WARACH S; TIJERINA ML; MILLER A; KEILSON M; DREXLER E; MORGANTE L; MANDELBAUM MA; HASSAN R; GORDON DL
      INTERPHYSICIAN AGREEMENT IN THE DIAGNOSIS OF SUBTYPES OF ACUTE ISCHEMIC STROKE - IMPLICATIONS FOR CLINICAL-TRIALS

      Neurology
    36. NANCE MA; PRATT VM; BOYADJIEV S; TAYLOR S; HODES ME; DLOUHY SR
      ADULT-ONSET NEUROLOGICAL DISORDER IN A PELIZAEUS-MERZBACHER DISEASE CARRIER MOTHER

      American journal of human genetics


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Documento generato il 31/05/20 alle ore 21:52:24