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La ricerca find articoli where soggetti phrase all words 'OPTIC ATROPHY' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 166 riferimenti
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    1. Barrett, TG
      Mitochondrial diabetes, DIDMOAD and other inherited diabetes syndromes

      BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM
    2. Griparic, L; van der Bliek, AM
      The many shapes of mitochondrial membranes

      TRAFFIC
    3. Torres, R; Leroy, E; Hu, X; Katrivanou, A; Gourzis, P; Papachatzopoulou, A; Athanassiadou, A; Beratis, S; Collier, D; Polymeropoulos, MH
      Mutation screening of the Wolfram syndrome gene in psychiatric patients

      MOLECULAR PSYCHIATRY
    4. Zeviani, M; Klopstock, T
      Mitochondrial disorders

      CURRENT OPINION IN NEUROLOGY
    5. Takeda, K; Inoue, H; Tanizawa, Y; Matsuzaki, Y; Oba, J; Watanabe, Y; Shinoda, K; Oka, Y
      WFS1 (Wolfram syndrome 1) gene product: predominant subcellular localization to endoplasmic reticulum in cultured cells and neuronal expression in rat brain

      HUMAN MOLECULAR GENETICS
    6. Bespalova, IN; Van Camp, G; Bom, SJH; Brown, DJ; Cryns, K; DeWan, AT; Erson, AE; Flothmann, K; Kunst, HPM; Kurnool, P; Sivakumaran, TA; Cremers, CWRJ; Leal, SM; Burmeister, M; Lesperance, MM
      Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss

      HUMAN MOLECULAR GENETICS
    7. Young, TL; Ives, E; Lynch, E; Person, R; Snook, S; MacLaren, L; Cator, T; Griffin, A; Fernandez, B; Lee, MK; King, MC
      Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1

      HUMAN MOLECULAR GENETICS
    8. Shoubridge, EA
      Nuclear genetic defects of oxidative phosphorylation

      HUMAN MOLECULAR GENETICS
    9. Yoon, Y; McNiven, MA
      Mitochondrial division: New partners in membrane pinching

      CURRENT BIOLOGY
    10. Sreekumar, KR; Aravind, L; Koonin, EV
      Computational analysis of human disease-associated genes and their proteinproducts

      CURRENT OPINION IN GENETICS & DEVELOPMENT
    11. Danino, D; Hinshaw, JE
      Dynamin family of mechanoenzymes

      CURRENT OPINION IN CELL BIOLOGY
    12. Baysal, BE; Rubinstein, WS; Taschner, PEM
      Phenotypic dichotomy in mitochondrial complex II genetic disorders

      JOURNAL OF MOLECULAR MEDICINE-JMM
    13. Hurle, B; Lane, K; Kenney, J; Tarantino, LM; Bucan, M; Brownstein, BH; Ornitz, DM
      Physical mapping of the mouse tilted locus identifies an association between human deafness loci DFNA6/14 and vestibular system development

      GENOMICS
    14. Evans, KL; Le Hellard, S; Morris, SW; Lawson, D; Whitton, C; Semple, CAM; Fantes, JA; Torrance, HS; Malloy, MP; Maule, JC; Humphray, SJ; Ross, MT; Bentley, DR; Muir, WJ; Blackwood, DHR; Porteous, DJ
      A 6.9-Mb high-resolution BAC/PAC contig of human 4p15.3-p16.1, a candidateregion for bipolar affective disorder

      GENOMICS
    15. Riikonen, R
      The PEHO syndrome

      BRAIN & DEVELOPMENT
    16. Vaher, U; Napa, A; Nurmiste, A; Piirsoo, A; Sibul, H; Talvik, T
      Four siblings with Hallervorden-Spatz disease

      BRAIN & DEVELOPMENT
    17. Ainsworth, JR; Morton, JE; Good, P; Woods, CG; George, NDL; Shield, JP; Bradbury, J; Henderson, MJ; Chhina, J
      Micro syndrome in muslim Pakistan children

      OPHTHALMOLOGY
    18. Chinnery, PF; Andrews, RM; Turnbull, DM; Howell, N
      Leber hereditary optic neuropathy: Does heteroplasmy influence the inheritance and expression of the G11778A mitochondrial DNA mutation?

      AMERICAN JOURNAL OF MEDICAL GENETICS
    19. Megarbane, A; Delague, V; Ruchoux, MM; Rizkallah, E; Maurage, CA; Viollet, L; Rouaix-Emery, N; Urtizberea, A
      New autosomal recessive cerebellar ataxia disorder in a large inbred Lebanese family

      AMERICAN JOURNAL OF MEDICAL GENETICS
    20. Hickman, SJ; Brex, PA; Brierley, CMH; Silver, NC; Barker, GJ; Scolding, NJ; Compston, DAS; Moseley, IF; Plant, GT; Miller, DH
      Detection of optic nerve atrophy following a single episode of unilateral optic neuritis by MRI using a fat-saturated short-echo fast FLAIR sequence

      NEURORADIOLOGY
    21. Schmidt, D; Lagreze, W; Vaith, P
      Ophthalmoscopic findings in 3 patients with panarteritis nodosa and reviewof the literature

      KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE
    22. Gemignani, F; Marbini, A
      Charcot-Marie-Tooth disease (CMT): distinctive phenotypic and genotypic features in CMT type 2

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    23. Senoo-Matsuda, N; Yasuda, K; Tsuda, M; Ohkubo, T; Yoshimura, S; Nakazawa, H; Hartman, PS; Ishii, N
      A defect in the cytochrome b large subunit in complex II causes both superoxide anion overproduction and abnormal energy metabolism in Caenorhabditiselegans

      JOURNAL OF BIOLOGICAL CHEMISTRY
    24. Sam, W; Qin, H; Crawford, B; Yue, D; Yu, S
      Homozygosity for a 4-bp deletion in a patient with Wolfram syndrome suggesting possible phenotype and genotype correlation

      CLINICAL GENETICS
    25. Chinnery, PF; Brown, DT; Andrews, RM; Singh-Kler, R; Riordan-Eva, P; Lindley, J; Applegarth, DA; Turnbull, DM; Howell, N
      The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy

      BRAIN
    26. Mudgil, AV; Repka, MX
      Childhood optic atrophy

      CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
    27. Pinckers, A; Uvijls, A
      The luminance fall in anomaloscope examination: clinical examples

      ACTA OPHTHALMOLOGICA SCANDINAVICA
    28. Bekir, NA; Gungor, K; Guran, S
      A DIDMOAD syndrome family with juvenile glaucoma and myopia findings

      ACTA OPHTHALMOLOGICA SCANDINAVICA
    29. Chen, AS; Kovach, MJ; Herman, K; Avakian, A; Frank, W; Forrester, S; Lin, JP; Kimonis, V
      Clinical heterogeneity in autosomal dominant optic atrophy in two 3q28-qter linked central Illinois families

      GENETICS IN MEDICINE
    30. Paterson, AD; Petronis, A
      Age of diagnosis-based linkage analysis in type 1 diabetes

      EUROPEAN JOURNAL OF HUMAN GENETICS
    31. Abdel-Salam, GMH; Svekus, A; Pelle, Z; Halasz, AA; Czeizel, AE
      Microcephaly, microphthalmia, congenital cataract, with calcification of the basal ganglia: MCA/MR syndrome

      GENETIC COUNSELING
    32. Wolfe, GI; Brower, RD; Burns, DK
      Perineurial cell hyperplasia in early-onset polyneuropathy with multiple cranial neuropathies

      NEUROMUSCULAR DISORDERS
    33. Shuper, A; Kornreich, L; Michowitz, S; Schwartz, M; Yaniv, I; Cohen, IJ
      Visual pathway tumors and hydrocephalus

      PEDIATRIC HEMATOLOGY AND ONCOLOGY
    34. Nores, JM; Biacabe, B; Bonfils, P
      Olfactory disorders and general pathologies. Analysis and literature review.

      REVUE DE MEDECINE INTERNE
    35. Miyama, S; Arimoto, K; Kimiya, S; Miyama, S
      Complicated hereditary spastic paraplegia with peripheral neuropathy, optic atrophy and mental retardation

      NEUROPEDIATRICS
    36. Nassogne, MC; Henrot, B; Saint-Martin, C; Kadhim, H; Dobyns, WB; Sebire, G
      Polymicrogyria and motor neuropathy in micro syndrome

      NEUROPEDIATRICS
    37. Lee, WB; O'Halloran, HS; Berger, JR
      Human immunodeficiency virus and bilateral optic atrophy

      NEURO-OPHTHALMOLOGY
    38. McFadzean, RM
      fMRI: Has it fulfilled it S function with respect to the visual system?

      NEURO-OPHTHALMOLOGY
    39. Eidlitz-Markus, T; Shuper, A
      Delayed visual loss after blunt head trauma

      NEURO-OPHTHALMOLOGY
    40. Steigleman, A; Hertle, RW; Jain, A; Caruso, RC
      Optic nerve and cortical atrophy in a patient with hyper-IgM syndrome

      NEURO-OPHTHALMOLOGY
    41. Ohtsuki, T; Ishiguro, H; Yoshikawa, T; Arinami, T
      WFS1 gene mutation search in depressive patients: detection of five missense polymorphisms but no association with depression or bipolar affective disorder

      JOURNAL OF AFFECTIVE DISORDERS
    42. Middle, F; Jones, I; McCandless, F; Barrett, T; Khanim, F; Owen, MJ; Lendon, C; Craddock, N
      Bipolar disorder and variation at a common polymorphism (A1832G) within exon 8 of the Wolfram gene

      AMERICAN JOURNAL OF MEDICAL GENETICS
    43. Evans, KL; Lawson, D; Meitinger, T; Blackwood, DHR; Porteous, DJ
      Mutational analysis of the Wolfram syndrome gene in two families with chromosome 4p-linked bipolar affective disorder

      AMERICAN JOURNAL OF MEDICAL GENETICS
    44. Pavone, P; Parano, E; Polizzi, A; Trifiletti, RR
      Colobomatous microphthalmia, microcephaly with cerebellar hypoplasia: Association or new syndrome?

      AMERICAN JOURNAL OF MEDICAL GENETICS
    45. Wein, F; Miller, NR; Vaphiades, MS
      An unusual homonymous visual field defect

      SURVEY OF OPHTHALMOLOGY
    46. Votruba, M; Leary, S; Losseff, N; Bhattacharya, SS; Moore, AT; Miller, DH; Moseley, IF
      MRI of the intraorbital optic nerve in patients with autosomal dominant optic atrophy

      NEURORADIOLOGY
    47. Riikonen, R; Vanhanen, SL; Tyynela, J; Santavuori, P; Turpeinen, U
      CSF insulin-like growth factor-1 in infantile neuronal ceroid lipofuscinosis

      NEUROLOGY
    48. Rohrbach, JM; Schlote, T; Strik, H; Bornemann, A
      Walker-Warburg Syndrome in an adult?

      KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE
    49. Swift, M; Swift, RG
      Psychiatric disorders and mutations at the Wolfram syndrome locus

      BIOLOGICAL PSYCHIATRY
    50. Awata, T; Inoue, K; Kurihara, S; Ohkubo, T; Inoue, I; Abe, T; Takino, H; Kanazawa, Y; Katayama, S
      Missense variations of the gene responsible for Wolfram syndrome (WFS1/wolframin) in Japanese: Possible contribution of the Arg456His mutation to type 1 diabetes as a nonautoimmune genetic basis

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    51. El-Shanti, H; Lidral, AC; Jarrah, N; Druhan, L; Ajlouni, K
      Homozygosity mapping identifies an additional locus for Wolfram syndrome on chromosome 4q

      AMERICAN JOURNAL OF HUMAN GENETICS
    52. Huna-Baron, R; Lesser, RJ; Warren, FA; Muszynski, CA; Kupersmith, MJ
      Infantile cerebral aneurysms with visual pathway compression

      PEDIATRIC NEUROSURGERY
    53. Nomura, S; Suzuki, R; Sugiyama, S; Nogami, K; Ito, H
      Optic glioma with characteristic bilateral optic atrophy in a 3-year-old girl

      PEDIATRIC NEUROSURGERY
    54. Criado, GR; Rufo, M; de Terreros, IG
      A second family with Micro syndrome

      CLINICAL DYSMORPHOLOGY
    55. Furlong, RA; Ho, LW; Rubinsztein, JS; Michael, A; Walsh, C; Paykel, ES; Rubinsztein, DC
      A rare coding variant within the wolframin gene in bipolar and unipolar affective disorder cases

      NEUROSCIENCE LETTERS
    56. Bacon, W; Hall, RK; Roset, JP; Boukari, A; Tenenbaum, H; Walter, B
      GAPO syndrome: a new case of this rare syndrome and a review of the relative importance of different phenotypic features in diagnosis

      JOURNAL OF CRANIOFACIAL GENETICS AND DEVELOPMENTAL BIOLOGY
    57. Kim, JY; Roh, JK
      Quadruple sectoranopia caused by posterior cerebral artery infarction

      NEURO-OPHTHALMOLOGY
    58. Baz, P; Azar, ST; Medlej, R; Bejjani, R; Halabi, G; Salti, I
      Role of early fundoscopy for diagnosis of Wolfram syndrome in type 1 diabetic patients

      DIABETES CARE
    59. Danesh-Meyer, H; Kubis, KC; Sergott, RC
      Not so slowly progressive visual loss

      SURVEY OF OPHTHALMOLOGY
    60. Galluzzi, P; Filosomi, G; Vallone, IM; Bardelli, AM; Venturi, C
      MRI of Wolfram syndrome (DIDMOAD)

      NEURORADIOLOGY
    61. Wenkel, H; Naumann, GOH
      Retrolaminar infiltration of optic nerve after silicone oil instillation after vitrectomy

      KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE
    62. Tekgul, S; Oge, O; Simsek, E; Yordam, N; Kendi, S
      Urological manifestations of the Wolfram syndrome: Observations in 14 patients

      JOURNAL OF UROLOGY
    63. Thomson, APJ; Neugebauer, M; Fryer, A
      Autosomal dominant optic atrophy with unilateral facial palsy: a new hereditary condition?

      JOURNAL OF MEDICAL GENETICS
    64. Ilker, SS; Ozturk, F; Kurt, E; Temel, M; Gul, D; Sayli, BS
      Ophthalmic findings in GAPO syndrome

      JAPANESE JOURNAL OF OPHTHALMOLOGY
    65. Gerbitz, KD
      Reflexions on a newly discovered diabetogenic gene, wolframin (WFS1)

      DIABETOLOGIA
    66. Nissenkorn, A; Zeharia, A; Lev, D; Fatal-Valevski, A; Barash, V; Gutman, A; Harel, S; Lerman-Sagie, T
      Multiple presentation of mitochondrial disorders

      ARCHIVES OF DISEASE IN CHILDHOOD
    67. Hardy, C; Khanim, F; Torres, R; Scott-Brown, M; Seller, A; Poulton, J; Collier, D; Kirk, J; Polymeropoulos, M; Latif, F; Barrett, T
      Clinical and molecular genetic analysis of 19 Wolfram syndrome kindreds demonstrating a wide spectrum of mutations in WFS1

      AMERICAN JOURNAL OF HUMAN GENETICS
    68. Shannon, P; Becker, L; Deck, J
      Evidence of widespread axonal pathology in Wolfram syndrome

      ACTA NEUROPATHOLOGICA
    69. LINDBLOM B; BONDTAYLOR L
      SCANNING LASER OPHTHALMOSCOPY AS A TOOL FOR DETECTING ATROPHY OF THE CENTRAL RETINAL NERVE-FIBER LAYER IN LEBERS HEREDITARY OPTIC NEUROPATHY

      Acta ophthalmologica Scandinavica
    70. Fein-Levy, C; Gorlick, R; Meyers, PA; Healey, J; Huvos, AG
      Ewing's sarcoma in a patient with congenital optic atrophy

      JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
    71. ALGAZALI LI
      MENTAL-RETARDATION, IRIS COLOBOMA, OPTIC ATROPHY AND DISTINCTIVE FACIAL APPEARANCE IN 2 SIBS

      Clinical dysmorphology
    72. RIGOLI L; ARRIGO T; CORIGLIANO G; DEGIORGI G; FRANZESE A; GIORGETTI R; LASCO A; LUCENTINI L; MARIETTI G; MARTINUCCI ME; PARRILLO M; PICCO P; IAFUSCO D; DELUCA F; CUCINOTTA D
      MITOCHONDRIAL-DNA STUDIES AND CLINICAL FINDINGS IN WOLFRAM-SYNDROME -AN ITALIAN MULTICENTER SURVEY

      Diabetes, nutrition & metabolism
    73. COSTEFF H; APTER N; ELPELEG ON; PRIALNIC M; BOHLES HJ
      INEFFECTIVENESS OF ORAL COENZYME-Q10 SUPPLEMENTATION IN 3-METHYLGLUTACONIC ACIDURIA, TYPE-3

      Brain & development
    74. Ohata, T; Koizumi, A; Kayo, T; Shoji, Y; Watanabe, A; Monoh, K; Higashi, K; Ito, S; Ogawa, O; Wada, Y; Takada, G
      Evidence of an increased risk of hearing loss in heterozygous carriers in a Wolfram syndrome family

      HUMAN GENETICS
    75. MUTHUKUMAR N; SUNDARALINGAM MP
      RETINOCEPHALIC VASCULAR MALFORMATION - CASE-REPORT

      British journal of neurosurgery
    76. BATTISTELLA PA; MIDENA E; SUPPIEJ A; CAROLLO C
      OPTIC ATROPHY AS THE FIRST SYMPTOM IN HALLERVORDEN-SPATZ-SYNDROME

      Child's nervous system
    77. Hajji, Z; Halhal, M; Chaoui, Z; Chefchaouni, M; Agnaou, L; Berraho, A
      Wolfram syndrome: 3 cases.

      JOURNAL FRANCAIS D OPHTALMOLOGIE
    78. STRAUSSBERG R; BRAND N; GADOTH N
      3-METHYL GLUTACONIC ACIDURIA IN IRAQI JEWISH CHILDREN MAYBE MISDIAGNOSED AS CEREBRAL-PALSY

      Neuropediatrics
    79. SABATELLI M; MIGNOGNA T; LIPPI G; SERVIDEI S; ZOLLINO M; PADUA L; LOMONACO M; DEARMAS L; MEREU ML; TONALI P
      HEREDITARY MOTOR AND SENSORY NEUROPATHY WITH DEAFNESS, MENTAL-RETARDATION, AND ABSENCE OF SENSORY LARGE MYELINATED FIBERS - CONFIRMATION OFA NEW ENTITY

      American journal of medical genetics
    80. Atchaneeyasakul, LO; Linck, LM; Connor, WE; Weleber, RG; Steiner, RD
      Eye findings in 8 children and a spontaneously aborted fetus with RSH/Smith-Lemli-Opitz syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    81. KRETSCHMANN U; SEELIGER M; RUETHER K; USUI T; ZRENNER E
      SPATIAL CONE ACTIVITY DISTRIBUTION IN DISEASES OF THE POSTERIOR POLE DETERMINED BY MULTIFOCAL ELECTRORETINOGRAPHY

      Vision research (Oxford)
    82. SIMUNOVIC MP; VOTRUBA M; REGAN BC; MOLLON JD
      COLOR DISCRIMINATION ELLIPSES IN PATIENTS WITH DOMINANT OPTIC ATROPHY

      Vision research (Oxford)
    83. KULKARNI AG; AMTE AP; BRID NS; YADAV SR
      BILATERAL OPTIC ATROPHY WITH HYDROCEPHALUS

      Postgraduate medical journal
    84. FRAMME C; HERBOTH T; ROIDER J; LAQUA H
      SUBRETINAL NEOVASCULAR MEMBRANES IN MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS TYPE-II

      Klinische Monatsblatter fur Augenheilkunde
    85. LEFEVRE A; HIROZ C; ZOGRAFOS L; SCHORDERET DF; MUNIER FL
      CLINICAL AND GENETIC DESCRIPTION OF 2 FAM ILIES WITH DOMINANT OPTIC ATROPHY OF KJIER (LOCUS 3Q28)

      Klinische Monatsblatter fur Augenheilkunde
    86. TEEBI AS; MILLER S; OSTRER H; EYDOUX P; COLOMBBROCKMANN C; OUDJHANE K; WATTERS G
      SPASTIC PARAPLEGIA, OPTIC ATROPHY, MICROCEPHALY WITH NORMAL INTELLIGENCE, AND XY SEX REVERSAL - A NEW AUTOSOMAL RECESSIVE SYNDROME

      Journal of Medical Genetics
    87. VOTRUBA M; MOORE AT; BHATTACHARYA SS
      CLINICAL-FEATURES, MOLECULAR-GENETICS, AND PATHOPHYSIOLOGY OF DOMINANT OPTIC ATROPHY

      Journal of Medical Genetics
    88. HARADA T; SAWAMURA Y; OHASHI T; HARADA C; SHINMEI Y; YOSHIDA K; MATSUDA H
      SEVERE OPTIC DISC EDEMA WITHOUT HYDROCEPHALUS IN NEUROFIBROMATOSIS-2

      Japanese Journal of Ophthalmology
    89. Holder, GE; Votruba, M; Carter, AC; Bhattacharya, SS; Fitzke, FW; Moore, AT
      Electrophysiological findings in dominant optic atrophy (DOA) linking to the OPA1 locus on chromosome 3q 28-qter

      DOCUMENTA OPHTHALMOLOGICA
    90. STOILOVA D; CHILD A; DESAI SP; SARFARAZI M
      REFINEMENT OF THE LOCUS FOR AUTOSOMAL-DOMINANT JUVENILE OPTIC ATROPHYTO A 2 CM REGION ON 3Q28

      Ophthalmic genetics
    91. IANNACCONE A; DEPROPRIS G; RONCATI S; RISPOLI E; DELPORTO G; PANNARALE MR
      THE OCULAR PHENOTYPE OF THE BARDET-BIEDL SYNDROME - COMPARISON TO NON-SYNDROMIC RETINITIS-PIGMENTOSA

      Ophthalmic genetics
    92. MIKI A; NAKAJIMA T; HASEBE H; ABE H
      FUNCTIONAL MAGNETIC-RESONANCE-IMAGING OF VISUAL FUNCTION IN POSTPAPILLEDEMA OPTIC ATROPHY

      Journal of neuro-ophthalmology
    93. ANDERSON DR; CYNADER MS
      GLAUCOMATOUS OPTIC-NERVE CUPPING AS AN OPTIC NEUROPATHY

      Clinical neuroscience
    94. OHTAGAKI A; HARA T; MAEGAKI Y; TAKESHITA K
      INTRACRANIAL CALCIFICATIONS, EPILEPSY, AND OPTIC ATROPHY ASSOCIATED WITH METAPHYSEAL DYSPLASIA - A CASE-REPORT

      Brain & development
    95. DILLMANN U; HEIDE G; DIETZ B; TESHMAR E; SCHIMRIGK K
      HEREDITARY MOTOR AND SENSORY NEUROPATHY WITH SPASTIC PARAPLEGIA AND OPTIC ATROPHY - REPORT ON A FAMILY

      Journal of neurology
    96. SUMBOONNANONDA A; VONGJIRAD A; SUNTORNPOCH V; ANGSUSINGHA K; PARICHATIKANOND P; LAOHAPAND T
      RENAL-FAILURE IN 2 PATIENTS WITH WOLFRAM-SYNDROME

      Journal of pediatric endocrinology & metabolism
    97. JAKOBS EM; ADELBERG DA; LEWIS JM; TRPIS M; GREEN WR
      OPHTHALMOMYIASIS INTERNA POSTERIOR - REPORT OF A CASE WITH OPTIC ATROPHY

      Retina
    98. BHANDARI A; FONTANA L; FITZKE FW; HITCHINGS RA
      QUANTITATIVE-ANALYSIS OF THE LAMINA-CRIBROSA IN-VIVO USING A SCANNINGLASER OPTHALMOSCOPE

      Current eye research
    99. STAVROU P; SGOUROS S; WILLSHAW HE; GOLDIN JH; HOCKLEY AD; WAKE MJC
      VISUAL FAILURE CAUSED BY RAISED INTRACRANIAL-PRESSURE IN CRANIOSYNOSTOSIS

      Child's nervous system
    100. GARTY BZ; SNIR M; KREMER I; YASSUR Y; TRATTNER A
      RETINAL CHANGES IN FAMILIAL PERIPHERAL SENSORY AND MOTOR NEUROPATHY ASSOCIATED WITH ANTERIOR CERVICAL HYPERTRICHOSIS

      Journal of pediatric ophthalmology and strabismus


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 19/01/21 alle ore 05:47:40