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    1. Sohocki, MM; Daiger, SP; Bowne, SJ; Rodriguez, JA; Northrup, H; Heckenlively, JR; Birch, DG; Mintz-Hittner, H; Ruiz, RS; Lewis, RA; Saperstein, DA; Sullivan, LS
      Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies

      HUMAN MUTATION
    2. Webster, AR; Heon, E; Lotery, AJ; Vandenburgh, K; Casavant, TL; Oh, KT; Beck, G; Fishman, GA; Lam, BL; Levin, A; Heckenlively, JR; Jacobson, SG; Weleber, RG; Sheffield, VC; Stone, EM
      An analysis of allelic variation in the ABCA4 gene

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    3. Tzekov, RT; Liu, YB; Sohocki, MM; Zack, DJ; Daiger, SP; Heckenlively, JR; Birch, DG
      Autosomal dominant retinal degeneration and bone loss in patients with a 12-bp deletion in the CRX gene

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    4. Stone, J; Maslim, J; Fawzi, AA; Lancaster, P; Heckenlively, JR
      The role of perinatal stress in simplex retinitis pigmentosa: evidence from surveys in Australia and the United States

      CANADIAN JOURNAL OF OPHTHALMOLOGY-JOURNAL CANADIEN D OPHTALMOLOGIE
    5. den Hollander, AI; Heckenlively, JR; van den Born, LI; de Kok, YJM; van der Velde-Visser, SD; Kellner, U; Jurklies, B; van Schooneveld, MJ; Blankenagel, A; Rohrschneider, K; Wissinger, B; Cruysberg, JRM; Deutman, AF; Brunner, HG; Apfeldstedt-Sylla, E; Hoyng, CB; Cremers, FPM
      Leber congenital amaurosis and retinitis pigmentosa with coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene

      AMERICAN JOURNAL OF HUMAN GENETICS
    6. Sohocki, MM; Perrault, I; Leroy, BP; Payne, AM; Dharmaraj, S; Bhattacharya, SS; Kaplan, J; Maumenee, IH; Koenekoop, R; Meire, FM; Birch, DG; Heckenlively, JR; Daiger, SP
      Prevalence of AIPL1 mutations in inherited retinal degenerative disease

      MOLECULAR GENETICS AND METABOLISM
    7. Slavotinek, AM; Stone, EM; Mykytyn, K; Heckenlively, JR; Green, JS; Heon, E; Musarella, MA; Parfrey, PS; Sheffield, VC; Biesecker, LG
      Mutations in MKKS cause Bardet-Biedl syndrome

      NATURE GENETICS
    8. Sohocki, MM; Bowne, SJ; Sullivan, LS; Blackshaw, S; Cepko, CL; Payne, AM; Bhattacharya, SS; Khaliq, S; Mehdi, SQ; Birch, DG; Harrison, WR; Elder, FFB; Heckenlively, JR; Daiger, SP
      Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenitalamaurosis

      NATURE GENETICS
    9. Ikeda, S; Shiva, N; Ikeda, A; Smith, RS; Nusinowitz, S; Yan, G; Lin, TR; Chu, S; Heckenlively, JR; North, MA; Naggert, JK; Nishina, PM; Duyao, MP
      Retinal degeneration but not obesity is observed in null mutants of the tubby-like protein 1 gene

      HUMAN MOLECULAR GENETICS
    10. Smith, RS; Hawes, NL; Chang, B; Roderick, TH; Akeson, EC; Heckenlively, JR; Gong, XH; Wang, X; Davisson, MT
      Lop12, a mutation in mouse Crygd causing lens opacity similar to human Coppock cataract

      GENOMICS
    11. Eifrig, DE; Heckenlively, JR; Smiddy, WE; Weleber, RG
      Diagnostic and therapeutic challenges

      RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES
    12. Milam, AH; Curcio, CA; Cideciyan, AV; Saxena, S; John, SK; Kruth, HS; Malek, G; Heckenlively, JR; Weleber, RG; Jacobson, SG
      Dominant late-onset retinal degeneration with regional variation of sub-retinal pigment epithelium deposits, retinal function, and photoreceptor degeneration

      OPHTHALMOLOGY
    13. Hawes, NL; Chang, B; Hageman, GS; Nusinowitz, S; Nishina, PM; Schneider, BS; Smith, RS; Roderick, TH; Davisson, MT; Heckenlively, JR
      Retinal degeneration 6 (rd6): A new mouse model for human retinitis punctata albescens

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    14. Sligh, JE; Levy, SE; Waymire, KG; Allard, P; Dillehay, DL; Nusinowitz, S; Heckenlively, JR; MacGregor, GR; Wallace, DC
      Maternal germ-line transmission of mutant mtDNAs from embryonic stem cell-derived chimeric mice

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    15. Akhmedov, NB; Piriev, NI; Chang, B; Rapoport, AL; Hawes, NL; Nishina, PM; Nusinowitz, S; Heckenlively, JR; Roderick, TH; Kozak, CA; Danciger, M; Davisson, MT; Farber, DB
      A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    16. Heckenlively, JR; Fawzi, AA; Oversier, J; Jordan, BL; Aptsiauri, N
      Autoimmune retinopathy - Patients with antirecoverin immunoreactivity and panretinal degeneration

      ARCHIVES OF OPHTHALMOLOGY
    17. Astuto, LM; Weston, MD; Carney, CA; Hoover, DM; Cremers, CWRJ; Wagenaar, M; Moller, C; Smith, RJH; Pieke-Dahl, S; Greenberg, J; Ramesar, R; Jacobson, SG; Ayuso, C; Heckenlively, JR; Tamayo, M; Gorin, MB; Reardon, W; Kimerling, WJ
      Genetic heterogeneity of Usher syndrome: Analysis of 151 families with Usher type I

      AMERICAN JOURNAL OF HUMAN GENETICS
    18. Mears, AJ; Hiriyanna, S; Vervoort, R; Yashar, B; Gieser, L; Fahrner, S; Daiger, SP; Heckenlively, JR; Sieving, PA; Wright, AF; Swaroop, A
      Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15

      AMERICAN JOURNAL OF HUMAN GENETICS
    19. Hawes, NL; Smith, RS; Chang, B; Davisson, M; Heckenlively, JR; John, SWM
      Mouse fundus photography and angiography: A catalogue of normal and mutantphenotypes

      MOLECULAR VISION
    20. Chang, B; Hawes, NL; Roderick, TH; Smith, RS; Heckenlively, JR; Horwitz, J; Davisson, MT
      Identification of a missense mutation in the alpha A-crystallin gene of the lop18 mouse

      MOLECULAR VISION
    21. den Hollander, AI; ten Brink, JB; de Kok, YJM; van Soest, S; van den Born, LI; van Driel, MA; van de Pol, DJR; Payne, AM; Bhattacharya, SS; Kellner, U; Hoyng, CB; Westerveld, A; Brunner, HG; Bleeker-Wagemakers, EM; Deutman, AF; Heckenlively, JR; Cremers, FPM; Bergen, AAB
      Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)

      NATURE GENETICS
    22. Sullivan, LS; Heckenlively, JR; Bowne, SJ; Zuo, J; Hide, WA; Gal, A; Denton, M; Inglehearn, CF; Blanton, SH; Daiger, SP
      Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa

      NATURE GENETICS
    23. Chang, B; Smith, RS; Hawes, NL; Anderson, MG; Zabaleta, A; Savinova, O; Roderick, TH; Heckenlively, JR; Davisson, MT; John, SWM
      Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice

      NATURE GENETICS
    24. Bowne, SJ; Daiger, SP; Hims, MM; Sohocki, MM; Malone, KA; McKie, AB; Heckenlively, JR; Birch, DG; Inglehearn, CF; Bhattacharya, SS; Bird, A; Sullivan, LS
      Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosa

      HUMAN MOLECULAR GENETICS
    25. van Soest, S; van Rossem, MJ; Heckenlively, JR; van den Born, LI; de Meulemeester, TMAMO; Vliex, S; de Jong, PTVM; Bleeker-Wagemakers, EM; Westerveld, A; Bergen, AAB
      Integrated genetic and physical map of the 1q3 -> q32.1 region, encompassing the RP12 locus, the F13B and HF1 genes, and the EEF1AL11 and RPL30 pseudogenes

      CYTOGENETICS AND CELL GENETICS
    26. Grover, S; Fishman, GA; Anderson, RJ; Tozatti, MSV; Heckenlively, JR; Weleber, RG; Edwards, AO; Brown, J
      Visual acuity impairment in patients with retinitis pigmentosa at age 45 years or older

      OPHTHALMOLOGY
    27. Bateman, JB; Ferreira, RC; Heckenlively, JR; Menkes, J
      Menkes disease - Reply

      OPHTHALMOLOGY
    28. Gao, YQ; Danciger, M; Longmuir, R; Piriev, NI; Zhao, DY; Heckenlively, JR; Fishman, GA; Weleber, RG; Jacobson, SG; Stone, EM; Farber, DB
      Screening of the gene encoding the alpha '-subunit of cone cGMP-PDE in patients with retinal degenerations

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    29. Nusinowitz, S; Ridder, W; HEckenlively, JR
      Rod multifocal electroretinograms in mice

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    30. Heckenlively, JR; Jordan, BL; Aptsiauri, N
      Association of antiretinal antibodies and cystoid macular edema in patients with retinitis pigmentosa

      AMERICAN JOURNAL OF OPHTHALMOLOGY
    31. FERREIRA RC; HECKENLIVELY JR; MENKES JH; BATEMAN JB
      MENKES DISEASE - NEW OCULAR AND ELECTRORETINOGRAPHIC FINDINGS

      Ophthalmology
    32. HECKENLIVELY JR
      LONG-TERM FOLLOW-UP OF STARGARDTS-DISEASE AND FUNDUS FLAVIMACULATUS -DISCUSSION

      Ophthalmology
    33. JOHN SWM; SMITH RS; SAVINOVA OV; HAWES NL; CHANG B; TURNBULL D; DAVISSON M; RODERICK TH; HECKENLIVELY JR
      ESSENTIAL IRIS ATROPHY, PIGMENT DISPERSION, AND GLAUCOMA IN DBA 2J MICE/

      Investigative ophthalmology & visual science
    34. SOHOCKI MM; SULLIVAN LS; MINTZHITTNER HA; BIRCH D; HECKENLIVELY JR; FREUND CL; MCINNES RR; DAIGER SP
      A RANGE OF CLINICAL PHENOTYPES ASSOCIATED WITH MUTATIONS IN CRX, A PHOTORECEPTOR TRANSCRIPTION-FACTOR GENE

      American journal of human genetics
    35. RODERICK TH; CHANG B; HAWES NL; HECKENLIVELY JR
      A NEW DOMINANT RETINAL DEGENERATION (RD4) ASSOCIATED WITH A CHROMOSOMAL INVERSION IN THE MOUSE

      Genomics
    36. CHANG B; HAWES NL; SMITH RS; HECKENLIVELY JR; DAVISSON MT; RODERICK TH
      CHROMOSOMAL LOCALIZATION OF A NEW MOUSE LENS OPACITY GENE (LOP18) (VOL 36, PG 171, 1996)

      Genomics
    37. DANCIGER M; HECKENLIVELY JR; WELEBER RG; SIEVING PA; JACOBSON SG; FARBER DB
      SCREENING FOR MUTATIONS IN THE GENES ENCODING THE 3 SUBUNITS OF ROD CGMP-PDE IN SMALL ARRP FAMILIES

      Investigative ophthalmology & visual science
    38. GEYER D; RODRIGUEZ IR; HEINZMANN C; KOJIS TL; FLODMAN P; SPENCE MA; TILLER GE; MAZURUK K; HECKENLIVELY JR; CHADER GJ; BATEMAN JB
      MAP REFINEMENT OF REGION 17P13.3 AND EVALUATION OF PIGMENT-EPITHELIUMDERIVED FACTOR (PEDF), A CANDIDATE GENE IN AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA

      Investigative ophthalmology & visual science
    39. NUSINOWITZ S; PENG C; HECKENLIVELY JR
      ROD AND CONE ELECTRORETINOGRAMS (ERGS) IN THE RD-3 MOUSE MODEL OF RETINAL DEGENERATION

      Investigative ophthalmology & visual science
    40. APTSIAURI N; JORDAN BL; LEVY R; HARGRAVE PA; HECKENLIVELY JR; SMITH WC
      EPITOPE MAPPING OF ANTI-ENOLASE ANTIBODIES IN PATIENTS WITH CAR SYNDROME, RETINITIS-PIGMENTOSA (RP), AND DIABETES, INVESTIGATING POSSIBLE AUTOIMMUNE COMPONENTS OF PATHOGENESIS

      Investigative ophthalmology & visual science
    41. DANCIGER M; HECKENLIVELY JR; WELEBER RG; SIEVING PA; FISHMAN GA; JACOBSON SG; FARBER DB
      2 PAIRS OF SEQUENCE VARIANTS IN THE GENE ENCODING THE ALPHA-SUBUNIT OF ROD CGMP-PDE - ONE PAIR HAS POSSIBLE PATHOLOGICAL SIGNIFICANCE AND THE OTHER REVEALS A EUROPEAN FOUNDER

      American journal of human genetics
    42. KIM RY; SCHWARTZ SD; HECKENLIVELY JR; GREGOR ZJ; COOLING RJ
      GIANT RETINAL TEAR AND RETINAL-DETACHMENT WITH UNDERLYING RETINITIS-PIGMENTOSA AND HEARING-LOSS

      Eye
    43. CHANG B; HAWES NL; SMITH RS; HECKENLIVELY JR; DAVISSON MT; RODERICK TH
      CHROMOSOMAL LOCALIZATION OF A NEW MOUSE LENS OPACITY GENE (LOP18)

      Genomics
    44. NUSINOWITZ S; WEISZ JM; WELEBER RG; HECKENLIVELY JR
      CHARACTERISTIC ELECTRORETINOGRAPHIC FINDINGS IN QUININE RETINAL TOXICITY

      Investigative ophthalmology & visual science
    45. CHANG B; HAGEMAN GS; HECKENLIVELY JR; HAWES NL; PENG C; RODERICK TH; DAVISSON MT
      A MOUSE MODEL FOR RETINITIS PUNCTATA ALBESCENS - A NEW PATHOLOGICAL FINDING FOR RETINAL WHITE DOTS

      Investigative ophthalmology & visual science
    46. DAIGER SP; SULLIVAN LS; BLANTON SH; GARCIA CA; BIRCH DG; HECKENLIVELY JR
      MODEL SYSTEM FOR LINKAGE TESTING IN FAMILIES WITH AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA

      Investigative ophthalmology & visual science
    47. HECKENLIVELY JR; APTSIAURI N; HARGRAVE PA
      ANTI-RETINAL PROTEIN ANTIBODIES ARE SIGNIFICANTLY PRESENT IN GASES OFCYSTOID MACULAR EDEMA WITH RETINITIS-PIGMENTOSA

      Investigative ophthalmology & visual science
    48. HECKENLIVELY JR; DAVISSON MT; RODERICK TH; CHANG B
      MOUSE MODELS AND GENETIC APPROACHES TO UNDERSTANDING RETINAL DISORDERS

      Investigative ophthalmology & visual science
    49. SYRQUIN MG; BHAVSAR AR; ENGSTROM RE; SCHWARTZ SD; SMALL KW; HECKENLIVELY JR; YOSHIZUMI MO; KREIGER AE
      RETRIEVING POSTERIORLY DISLOCATED SILICONE LENSES VIA A PARS-PLANA APPROACH

      Investigative ophthalmology & visual science
    50. HAWES NL; RODERICK TH; CHANG B; HECKENLIVELY JR
      MOUSE CATARACT MODELS - CHARACTERIZATION AND LINKAGE DATA

      Investigative ophthalmology & visual science
    51. HEINZMANN C; KOJIS TL; FLODMAN P; TILLER GE; HECKENLIVELY JR; RODRIGUEZ IR; CHADER GJ; SPENCE MA; BATEMAN JB
      FINE MAPPING OF AN AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA (ADRP) LOCUS ON CHROMOSOME 17P13.3 AND ANALYSIS OF A CANDIDATE GENE

      Investigative ophthalmology & visual science
    52. SMITH RS; HAWES NL; KUHLMANN SD; HECKENLIVELY JR; CHANG B; RODERICK TH; SUNDBERG JP
      CORN1 - A MOUSE MODEL FOR CORNEAL SURFACE DISEASE AND NEOVASCULARIZATION

      Investigative ophthalmology & visual science
    53. KOJIS TL; HEINZMANN C; FLODMAN P; NGO JT; SPARKES RS; SPENCE MA; BATEMAN JB; HECKENLIVELY JR
      MAP REFINEMENT OF LOCUS RP13 TO HUMAN-CHROMOSOME 17P13.3 IN A 2ND FAMILY WITH AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA

      American journal of human genetics
    54. DAIGER SP; MCGUIRE RE; HECKENLIVELY JR
      THE MAP IS NOT THE TERRITORY - REPLY

      American journal of human genetics
    55. BASCOM RA; LIU L; HECKENLIVELY JR; STONE EM; MCINNES RR
      MUTATION ANALYSIS OF THE ROM1 GENE IN RETINITIS-PIGMENTOSA (VOL 4, PG1895, 1995)

      Human molecular genetics
    56. BASCOM RA; LIU L; HECKENLIVELY JR; STONE EM; MCINNES RR
      MUTATION ANALYSIS OF THE ROM1 GENE IN RETINITIS-PIGMENTOSA

      Human molecular genetics
    57. DANCIGER M; BLANEY J; GAO YQ; ZHAO DY; HECKENLIVELY JR; JACOBSON SG; FARBER DB
      MUTATIONS IN THE PDE6B GENE IN AUTOSOMAL RECESSIVE RETINITIS-PIGMENTOSA

      Genomics
    58. SULLIVAN LS; BLANTON SH; WAGNER MJ; HECKENLIVELY JR; DAIGER SP
      REFINED LINKAGE AND PHYSICAL MAPPING OF THE CHROMOSOME-8 FORM OF AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA (RP1)

      Cytogenetics and cell genetics
    59. HECKENLIVELY JR; TOWNSEND W; VERDON W
      SENILE PANRETINAL CONE DEGENERATION

      Investigative ophthalmology & visual science
    60. SHIN GS; BATEMAN JB; HECKENLIVELY JR; VERDON WA
      ELECTRORETINOGRAPHIC FEATURES OF ANIRIDIA

      Investigative ophthalmology & visual science
    61. PENG C; HAGEMAN GS; CHANG B; HECKENLIVELY JR
      ELECTRORETINOGRAPHIC ABNORMALITIES IN RD5 HETEROZYGOUS MICE - COMPARISON TO HOMOZYGOUS AND NORMAL CONTROLS

      Investigative ophthalmology & visual science
    62. SULLIVAN LS; BLANTON SH; WAGNER MJ; HECKENLIVELY JR; DAIGER SP
      FINE-STRUCTURE LINKAGE AND PHYSICAL MAPPING OF THE RP1 FORM OF AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA

      Investigative ophthalmology & visual science
    63. DAIGER SP; MCGUIRE RE; SULLIVAN LS; HECKENLIVELY JR
      X-LINKED DOMINANT CONE-ROD DYSTROPHY - LINKAGE MAPPING OF A NEW LOCUS(CORD3) TO XP22.13-P22.11

      Investigative ophthalmology & visual science
    64. HECKENLIVELY JR; CHANG B; ERWAY LC; PENG C; HAWES NL; HAGEMAN GS; RODERICK TH
      MOUSE MODEL FOR USHER SYNDROME - LINKAGE MAPPING SUGGESTS HOMOLOGY TOUSHER TYPE-I REPORTED AT HUMAN-CHROMOSOME 11P15

      Proceedings of the National Academy of Sciences of the United Statesof America
    65. KOJIS RI; HEINZMANN C; HECKENLIVELY JR; FLODMAN P; NGO JT; SPENCE MA; SPARKES RS; BATEMAN JB
      MAP REFINEMENT OF THE AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA (ADRP) LOCUS RP13 TO HUMAN-CHROMOSOME

      American journal of human genetics
    66. MCGUIRE RE; SULLIVAN LS; BLANTON SH; CHURCH MW; HECKENLIVELY JR; DAIGER SP
      X-LINKED DOMINANT CONE-ROD DEGENERATION - LINKAGE MAPPING OF A NEW LOCUS FOR RETINITIS-PIGMENTOSA (RP15) TO XP22.13-P22.11

      American journal of human genetics
    67. FISHMAN GA; STONE E; GILBERT LD; VANDENBURGH K; SHEFFIELD VC; HECKENLIVELY JR
      CLINICAL-FEATURES OF A PREVIOUSLY UNDESCRIBED CODON-216 (PROLINE TO SERINE) MUTATION IN THE PERIPHERIN RETINAL DEGENERATION SLOW GENE IN AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA/

      Ophthalmology
    68. LOGANI SC; LOGANI S; TANJI T; HECKENLIVELY JR
      RETROSPECTIVE CLINICAL REVIEW OF SUPRANORMAL ELECTRORETINOGRAPHIC RESPONSES

      Investigative ophthalmology & visual science
    69. LINBERG KA; FARISS RN; HECKENLIVELY JR; PENG C; BOWES C; FARBER DB; FISHER SK
      STRUCTURAL-CHANGES IN THE DEVELOPING RETINA OF THE RD-3 MOUSE

      Investigative ophthalmology & visual science
    70. FARISS RN; LINBERG KA; LO GJ; HECKENLIVELY JR; PENG C; FISHER SK
      RETINAL DEGENERATION IN THE RD-3 MOUSE LEADS TO CHANGES IN THE IMMUNOLOCALIZATION OF MULLER CELL AND PHOTORECEPTOR PROTEINS

      Investigative ophthalmology & visual science
    71. PENG C; HECKENLIVELY JR; CHANG B
      CHANGES IN ERG A-WAVE MAXIMUM VELOCITY IN RETINAL DEGENERATION MOUSE C57BL 6J-MND MND/

      Investigative ophthalmology & visual science
    72. HECKENLIVELY JR; CHANG B; RODERICK TH; PENG C; ERWAY LC
      A MOUSE MODEL FOR USHER SYNDROME

      Investigative ophthalmology & visual science
    73. CHANG B; BRONSON RT; HAWES NL; RODERICK TH; PENG C; HAGEMAN GS; HECKENLIVELY JR
      RETINAL DEGENERATION IN MOTOR-NEURON DEGENERATION - A MOUSE MODEL OF CEROID-LIPOFUSCINOSIS

      Investigative ophthalmology & visual science
    74. SADLER LA; GANNON AM; BLANTON SH; COTTINGHAM RW; WAGNER M; HECKENLIVELY JR; DAIGER SP
      LINKAGE AND PHYSICAL MAPPING OF THE CHROMOSOME-8 FORM OF AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA (RP1)

      Cytogenetics and cell genetics
    75. ADAMUS G; APTSIAURI N; GUY J; HECKENLIVELY JR; HARGRAVE PA
      ANTI-ENOLASE ANTIBODIES IN PARANEOPLASTIC RETINOPATHY

      The Journal of immunology
    76. HECKENLIVELY JR
      THE EVOLVING ROLE OF VISUAL ELECTRODIAGNOSTICS

      British journal of ophthalmology
    77. NATHANS J; MAUMENEE IH; ZRENNER E; SADOWSKI B; SHARPE LT; LEWIS RA; HANSEN E; ROSENBERG T; SCHWARTZ M; HECKENLIVELY JR; TRABOULSI E; KLINGAMAN R; BECHHANSEN NT; LAROCHE GR; PAGON RA; MURPHEY WH; WELEBER RG
      GENETIC-HETEROGENEITY AMONG BLUE-CONE MONOCHROMATES

      American journal of human genetics
    78. SADLER LA; BLANTON SH; COTTINGHAM RA; CRAFT CM; SWAROOP A; WAGNER MJ; HECKENLIVELY JR; DAIGER SP
      LINKAGE MAPPING OF ONE FORM (RP1) OF AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA TO 8Q11-Q21 AND EXCLUSION OF CANDIDATE GENES

      American journal of human genetics
    79. GANNON AM; RODRIGUEZ JA; HUMPHRIES P; BIRCH DG; HECKENLIVELY JR; DAIGER SP
      MUTATIONS IN PERIPHERIN RDS IN PATIENTS WITH RETINITIS-PIGMENTOSA - A12 BASE-PAIR DELETION IN EXON-2

      American journal of human genetics
    80. RODRIGUEZ JA; HERRERA CA; BIRCH DG; HECKENLIVELY JR; DAIGER SP
      RHODOPSIN MUTATIONS IN PATIENTS WITH RETINITIS-PIGMENTOSA

      American journal of human genetics
    81. RODERICK TH; HAWES NL; HECKENLIVELY JR; CHANG B; LANGLEY SH; HILLYARD AL
      LINKAGE OF 8 EYE LOCI IN THE MOUSE AND THE EYE GENETIC-MAP OF THE MOUSE

      Investigative ophthalmology & visual science
    82. HECKENLIVELY JR; CHANG B; HAWES NL; RODERICK TH
      2 NEW MOUSE RETINAL PRIMARY DEGENERATIONS

      Investigative ophthalmology & visual science
    83. LEHMER JM; HECKENLIVELY JR; STONE EM; KIMURA AE; BLANTON SH; DAIGER SP
      CLINICAL CHARACTERIZATION OF CHROMOSOME-8 AUTOSOMAL DOMINANT RETINITIS-PIGMENTOSA (UCLA-RP01)

      Investigative ophthalmology & visual science


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Documento generato il 20/10/20 alle ore 14:35:41