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La ricerca find articoli where soggetti phrase all words 'HYPERTELORISM' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 78 riferimenti
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    1. Ozek, C; Gundogan, H; Bilkay, U; Cankayali, R; Guner, U; Gurler, T; Songur, E
      Rare craniofacial anomaly: Tessier no. 2 cleft

      JOURNAL OF CRANIOFACIAL SURGERY
    2. Holmes, AD; Meara, JG; Kolker, AR; Rosenfeld, JV; Klug, GL
      Frontoethmoidal encephaloceles: Reconstruction and refinements

      JOURNAL OF CRANIOFACIAL SURGERY
    3. Goodrich, JT; Tutino, M
      An annotated history of craniofacial surgery and intentional cranial deformation

      NEUROSURGERY CLINICS OF NORTH AMERICA
    4. Evereklioglu, C; Doganay, S; Er, H; Tercan, M; Gunduz, A; Balat, A; Borazan, M
      Interpupillary index: a new parameter for hypo-hypertelorism

      JOURNAL OF CRANIO-MAXILLOFACIAL SURGERY
    5. Abdel-Meguid, N; Ashour, AM
      Holoprosencephaly and split hand/foot: an additional case with this rare association

      CLINICAL DYSMORPHOLOGY
    6. Dollfus, H; Cantenot, L; Rouault, F; Philipp, N; Flament, J
      Bilateral iridoretinal colobomas in a child with a Noonan phenotype

      CLINICAL DYSMORPHOLOGY
    7. Der Kaloustian, VM; Pelletier, M; Costa, T; Blackston, DR; Oudjhane, K
      A new syndrome with craniofacial and skeletal dysmorphisms and developmental delay

      CLINICAL DYSMORPHOLOGY
    8. Megarbane, A
      A new familial syndrome with facial abnormalities, abnormal EEG, and mental retardation

      CLINICAL DYSMORPHOLOGY
    9. Amiel, J; Faivre, L; Marianowskl, R; Bonnet, D; Couly, G; Manach, Y; Le Merrer, M; Cormier-Daire, V; Munnich, A; Lyonnet, S
      Hypertelorism-Microtia-Clefting Syndrome (Bixler syndrome): report of two unrelated cases

      CLINICAL DYSMORPHOLOGY
    10. Rudolph, G; Haritoglou, C; Kalpadakis, P; Boergen, KF; Meitinger, T
      LEOPARD syndrome with iris-retina-choroid coloboma

      OPHTHALMOLOGE
    11. Boonvisut, S; Ladpli, S; Sujatanond, M; Tisavipat, N; Luxsuwong, M; Nunta-aree, S; Boonampol, D; Srimaharaja, S; Panitphong, T; Dulayajinda, D; Areewattana, S
      A new technique for the repair and reconstruction of frontoethmoidal encephalomeningoceles by medial orbital composite-unit translocation

      BRITISH JOURNAL OF PLASTIC SURGERY
    12. Avunduk, AM; Aslan, Y; Kapicioglu, Z; Elmas, R
      High myopia, hypertelorism, iris coloboma, exomphalos, absent corpus callosum, and sensorineural deafness: Report of a case and further evidence for autosomal recessive inheritance

      ACTA OPHTHALMOLOGICA SCANDINAVICA
    13. Cook, K; Prefumo, F; Presti, F; Homfray, T; Campbell, S
      The prenatal diagnosis of Binder syndrome before 24 weeks of gestation: case report

      ULTRASOUND IN OBSTETRICS & GYNECOLOGY
    14. Majewski, F
      Lenz-Majewski hyperostotic dwarfism: Reexamination of the original patient

      AMERICAN JOURNAL OF MEDICAL GENETICS
    15. Jabre, A; Tabaddor, R; Samaraweera, R
      Transsphenoidal meningoencephalocele in adults

      SURGICAL NEUROLOGY
    16. Huang, TS; Elias, ER; Mulliken, JB; Kirse, DJ; Holmes, LB
      A new syndrome: Heart defects, laryngeal anomalies, preaxial polydactyly, and colonic aganglionosis in sibs

      GENETICS IN MEDICINE
    17. Eppley, BL; Hathaway, RR; Kalsbeck, JE; Rosenthal, M
      Craniofacial correction of giant frontoethmoidal encephalomeningocele

      JOURNAL OF CRANIOFACIAL SURGERY
    18. Songur, E; Mutluer, S; Gurler, T; Bilkay, U; Gorken, C; Guner, U; Celik, N
      Management of frontoethmoidal (sincipital) encephalocele

      JOURNAL OF CRANIOFACIAL SURGERY
    19. Liew, S; Poole, M; Kenton-Smith, J; Tan, S
      Orbital and globe rotation: the role of the periorbita

      JOURNAL OF CRANIO-MAXILLOFACIAL SURGERY
    20. Hu, D; Helms, JA
      The role of Sonic hedgehog in normal and abnormal craniofacial morphogenesis

      DEVELOPMENT
    21. Marchac, D; Arnaud, E
      Midface surgery from Tessier to distraction

      CHILDS NERVOUS SYSTEM
    22. Crisponi, G; Marras, AR; Corrias, A
      Two sibs with Malpuech syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    23. Megarbane, A; Stephan, E; Kassab, R; Ashoush, R; Salem, N; Bouvagnet, P; Loiselet, J
      Autosomal dominant secundum atrial septal defect with various cardiac and noncardiac defects: A new midline disorder

      AMERICAN JOURNAL OF MEDICAL GENETICS
    24. Slaney, SF; Goodman, FR; Eilers-Walsman, BLC; Hall, BD; Williams, DK; Young, ID; Hayward, RD; Jones, BM; Christianson, AL; Winter, RM
      Acromelic frontonasal dysostosis

      AMERICAN JOURNAL OF MEDICAL GENETICS
    25. Panchal, J; Kim, YO; Stelnicki, E; Pilgam, T; Marsh, JL
      Quantitative assessment of osseous, ocular, and periocular changes after hypertelorism surgery

      PLASTIC AND RECONSTRUCTIVE SURGERY
    26. Barretto, RL; Mathog, RH
      Orbital measurement in black and white populations

      LARYNGOSCOPE
    27. Cario, H; Bode, H; Gustavsson, P; Dahl, N; Kohne, E
      A microdeletion syndrome due to a 3-Mb deletion on 19q13.2 - Diamond-Blackfan anemia associated with macrocephaly, hypotonia, and psychomotor retardation

      CLINICAL GENETICS
    28. Pivnick, EK; Rivas, ML; Tolley, EA; Smith, SD; Presbury, GJ
      Interpupillary distance in a normal black population

      CLINICAL GENETICS
    29. ALGAZALI LI
      MENTAL-RETARDATION, IRIS COLOBOMA, OPTIC ATROPHY AND DISTINCTIVE FACIAL APPEARANCE IN 2 SIBS

      Clinical dysmorphology
    30. IMAIZUMI K; ISHII T; MASUNO M; KUROKI Y
      ASSOCIATION OF HOLOPROSENCEPHALY, ECTRODACTYLY, CLEFT-LIP CLEFT-PALATE AND HYPERTELORISM - A POSSIBLE 3RD CASE

      Clinical dysmorphology
    31. JACOBSON Z; GLICKSTEIN J; HENSLE T; MARION RW
      FURTHER DELINEATION OF THE OPITZ-G BBB-SYNDROME - REPORT OF AN INFANTWITH COMPLEX CONGENITAL HEART-DISEASE AND BLADDER EXSTROPHY, AND REVIEW OF THE LITERATURE/

      American journal of medical genetics
    32. NAKAGAWA M; KONDO M; MATSUI A
      TEEBI-HYPERTELORISM-SYNDROME WITH TETRALOGY OF FALLOT

      American journal of medical genetics
    33. MEHES K
      ISOLATED HYPOSPADIAS IS NOT ASSOCIATED WITH SIGNS OF MIDLINE CLOSURE DEFECTS

      American journal of medical genetics
    34. DESILVA D; OSBORNE A; SIMPSON SA; DEAN JCS; SEATON A
      OPITZ OCULO-GENITO-LARYNGEAL SYNDROME - A RARE CAUSE OF RECURRENT ASPIRATION PNEUMONIA IN AN ADULT

      Thorax
    35. PARK VM; PIVNICK EK
      NEUROFIBROMATOSIS TYPE-1 (NF1) - A PROTEIN TRUNCATION ASSAY YIELDING IDENTIFICATION OF MUTATIONS IN 73-PERCENT OF PATIENTS

      Journal of Medical Genetics
    36. DEPONTE FS; BOTTINI DJ; SASSANO PP; IANNETTI G
      SURGICAL PLANNING AND CORRECTION OF MEDIAL CRANIOFACIAL CLEFT

      The Journal of craniofacial surgery
    37. SONGUR E; MUTLUER S; KECECI Y; ALPER M; GUNER U; TOTAN S
      LATE RESULTS OF HYPERTELORISM CORRECTION

      The Journal of craniofacial surgery
    38. HOVING EW; VERMEIJKEERS C
      FRONTOETHMOIDAL ENCEPHALOCELES, A STUDY OF THEIR PATHOGENESIS

      Pediatric neurosurgery
    39. MEGARBANE A; LEMERRER M; ELKALLAB K
      PTOSIS, DOWN-SLANTING PALPEBRAL FISSURES, HYPERTELORISM, SEIZURES ANDMENTAL-RETARDATION - A POSSIBLE NEW MCA MR SYNDROME/

      Clinical dysmorphology
    40. LOPES VLGD; CAMPOS NLV; MACIELGUERRA AT
      CRANIO-OCULO-FRONTO-NASAL MALFORMATION - A NEW MCA CONDITION

      Clinical dysmorphology
    41. DELCAMPO AF
      A SIMPLE PROCEDURE FOR AESTHETIC CORRECTION OF THE MEDIAL EPICANTHAL FOLD

      Aesthetic plastic surgery
    42. NEVIN NC; CRAIG BG; MULLHOLLAND HC; CASEY F
      CLEFT-LIP AND PALATE, HYPERTELORISM, BRACHYCEPHALY, FLAT FACIAL PROFILE, AND CONGENITAL HEART-DISEASE IN 3 BROTHERS

      American journal of medical genetics
    43. WALLERSTEIN R; SCOTT CI; NICHOLSON L
      EXTENDED SURVIVAL IN A NEW CASE OF TER HAAR SYNDROME - FURTHER DELINEATION OF THE SYNDROME

      American journal of medical genetics
    44. SCHOWALTER DB; PAGON RA; KALINA RE; MCDONALD R
      FACIO-OCULO-ACOUSTICO-RENAL (FOAR) SYNDROME - CASE-REPORT AND REVIEW

      American journal of medical genetics
    45. GRIPP KW; DONNAI D; CLERICUZIO CL; MCDONALDMCGINN DM; GUTTENBERG M; ZACKAI EH
      DIAPHRAGMATIC HERNIA-EXOMPHALOS-HYPERTELORISM SYNDROME - A NEW CASE AND FURTHER EVIDENCE OF AUTOSOMAL RECESSIVE INHERITANCE

      American journal of medical genetics
    46. TAR A; ION A; SOLYOM J; GYORVARI B; STEPHENSON C; BARBAUX S; NUNES M; FELLOUS M; MCELREAVEY K
      HYPERTELORISM AND HYPOSPADIAS ASSOCIATED WITH A DE-NOVO APPARENTLY BALANCED TRANSLOCATION BETWEEN 8Q22.3-23 AND 20P13

      American journal of medical genetics
    47. MAY M; HUSTON S; WILROY RS; SCHWARTZ C
      LINKAGE ANALYSIS IN A FAMILY WITH THE OPITZ GBBB SYNDROME REFINES THELOCATION OF THE GENE IN XP22 TO A 4 CM REGION

      American journal of medical genetics
    48. TAN ST; MULLIKEN JB
      HYPERTELORISM - NOSOLOGIC ANALYSIS OF 90 PATIENTS

      Plastic and reconstructive surgery
    49. ORR DJA; SLANEY S; ASHWORTH GJ; POOLE MD
      CRANIOFRONTONASAL DYSPLASIA

      British Journal of Plastic Surgery
    50. GORLIN RJ; WIEDEMANN HR
      BLEPHARO-CHEILO-DONTIC (BCD) SYNDROME

      Acta ophthalmologica Scandinavica
    51. ANASTASSOV GE; VANDAMME PA
      ORBITOMETER-OPHTHALMOMETER - NEW SURGICAL AND CLINICAL DEVICE

      The Journal of craniofacial surgery
    52. FADDA MT; DEPONTE FS; BOTTINI DJ; IANNETTI G
      STUDY AND PLANNING OF THE SURGICAL-PROCEDURE FOR THE ORBITAL DISTRICTIN PATIENTS AFFECTED BY CRANIOFACIAL MALFORMATIONS

      The Journal of craniofacial surgery
    53. COHEN MM; KREIBORG S
      A CLINICAL-STUDY OF THE CRANIOFACIAL FEATURES IN APERT SYNDROME

      International journal of oral and maxillofacial surgery
    54. ROBIN NH; OPITZ JM; MUENKE M
      OPITZ G BBB SYNDROME - CLINICAL COMPARISONS OF FAMILIES LINKED TO XP22 AND 22Q, AND A REVIEW OF THE LITERATURE/

      American journal of medical genetics
    55. MCPHERSON E; CLEMENS M
      CLEFT-LIP AND PALATE, CHARACTERISTIC FACIAL APPEARANCE, MALROTATION OF THE INTESTINE, AND LETHAL CONGENITAL HEART-DISEASE IN 2 SIBS - A NEWAUTOSOMAL RECESSIVE CONDITION

      American journal of medical genetics
    56. GUIONALMEIDA ML; RICHIERICOSTA A; SAAVEDRA D; COHEN MM
      CEREBROFACIOTHORACIC SYNDROME

      American journal of medical genetics
    57. MACFARLANE R; RUTKA JT; ARMSTRONG D; PHILIPS J; POSNICK J; FORTE V; HUMPHREYS RP; DRAKE J; HOFFMAN HJ
      ENCEPHALOCELES OF THE ANTERIOR CRANIAL FOSSA - MANAGEMENT AND OUTCOME

      Pediatric neurosurgery
    58. ROSANOWSKI F; TIGGES M; EYSHOLDT U
      INHERITED BILATERAL ATRESIA OF THE EXTERN AL AUDITORY-CANAL AND HYPERTELORISM

      Laryngo-, Rhino-, Otologie
    59. CHINEN Y; NARITOMI K
      MALPUECH FACIAL CLEFTING SYNDROME IN A JAPANESE BOY WITH CARDIAC DEFECTS

      Japanese journal of human genetics
    60. COHEN MM; RICHIERICOSTA A; GUIONALMEIDA ML; SAAVEDRA D
      HYPERTELORISM - INTERORBITAL GROWTH, MEASUREMENTS, AND PATHOGENETIC CONSIDERATIONS

      International journal of oral and maxillofacial surgery
    61. ROUSSAT B; CHOUKROUN JB; DARBOIS Y
      ANTENATAL SONOGRAPHIC STUDY OF THE EYE

      Journal francais d'ophtalmologie
    62. MERZ E; WELLEK S; PUTTMANN S; BAHLMANN F; WEBER G
      ORBITAL DIAMETER, INTERORBITAL AND BIOCUL AR DIAMETERS - A GROWTH-MODEL FOR FETAL ORBITAL PARAMETERS

      Ultraschall in der Medizin
    63. TSUKAHARA M; UCHIDA M; SHINOHARA T
      TEEBI HYPERTELORISM SYNDROME - FURTHER OBSERVATIONS

      American journal of medical genetics
    64. VERLOES A; DAVID A; ODENT S; TOUTAIN A; ANDRE MJ; LUCAS J; LEMAREC B
      OPITZ GBBB SYNDROME - CHROMOSOMAL EVIDENCE OF AN X-LINKED FORM

      American journal of medical genetics
    65. TEEBI AS; QUMSIYEH MB; MEYERSSEIFER CH; MEYN MS
      VELO-FACIO-SKELETAL SYNDROME IN A MOTHER AND DAUGHTER

      American journal of medical genetics
    66. GUIONALMEIDA ML; RODINI ESO
      MICHELS SYNDROME IN A BRAZILIAN GIRL BORN TO CONSANGUINEOUS PARENTS

      American journal of medical genetics
    67. RAMER JC; LIN AE; DOBYNS WB; WINTER R; AYME S; PALLOTTA R; LADDA RL
      PREVIOUSLY APPARENTLY UNDESCRIBED SYNDROME - SHALLOW ORBITS, PTOSIS, COLOBOMA, TRIGONOCEPHALY, GYRAL MALFORMATIONS, AND MENTAL AND GROWTH-RETARDATION

      American journal of medical genetics
    68. WYNNE SE; ALDRED MJ; BARTOLD PM
      HEREDITARY GINGIVAL FIBROMATOSIS ASSOCIATED WITH HEARING-LOSS AND SUPERNUMERARY TEETH - A NEW SYNDROME

      Journal of periodontology
    69. CONLON BJ; ODWYER T
      THE G-SYNDROME - OPITZ OCULO-GENITAL-LARYNGEAL SYNDROME - OPITZ BBB GSYNDROME - OPITZ-FRIAS SYNDROME/

      Journal of Laryngology and Otology
    70. PIZIO HF; SCOTT MH; RICHARD JM
      TORTUOSITY OF THE RETINAL-VESSELS IN AARSKOG SYNDROME (FACIOGENITAL-DYSPLASIA)

      Ophthalmic genetics
    71. TROUT T; BUDORICK NE; PRETORIUS DH; MCGAHAN JP
      SIGNIFICANCE OF ORBITAL MEASUREMENTS IN THE FETUS

      Journal of ultrasound in medicine
    72. MAHAPATRA AK; TANDON PN; DHAWAN IK; KHAZANCHI RK
      ANTERIOR ENCEPHALOCELES - A REPORT OF 30 CASES

      Child's nervous system
    73. MARTINEZFRIAS ML; BERMEJO E; OTERO TS; URIOSTE M; MORENA V; CRUZ E
      NEW SYNDROME - SCLEROCORNEA, HYPERTELORISM, SYNDACTYLY, AND AMBIGUOUSGENITALIA

      American journal of medical genetics
    74. WOLFF G; ZIMMERMANN E; ZIMMERHACKL B; HARNASCH C; JUNG C; BACK E
      2 BROTHERS WITH CHARACTERISTIC FACIAL APPEARANCE, SEVERE PSYCHOMOTOR RETARDATION, HYPOSPADIAS, CONTRACTURES, AND OTHER SYMPTOMS - A NEW RECESSIVE SYNDROME

      Journal of Medical Genetics
    75. MACDONALD MR; SCHAEFER GB; OLNEY AH; TAMAYO M; FRIAS JL
      BRAIN MAGNETIC-RESONANCE-IMAGING FINDINGS IN THE OPITZ G BBB SYNDROME- EXTENSION OF THE SPECTRUM OF MIDLINE BRAIN ANOMALIES/

      American journal of medical genetics
    76. TEEBI AS; RUCQUOI JK; MEYN MS
      AARSKOG SYNDROME - REPORT OF A FAMILY WITH REVIEW AND DISCUSSION OF NOSOLOGY

      American journal of medical genetics
    77. HAMMER B; PREIN J
      RECONSTRUCTIVE SURGERY IN THE ORBITAL REG ION

      Klinische Monatsblatter fur Augenheilkunde
    78. ANTONYSHYN OM; PALETZ JL; WILSON KL
      RECONSTRUCTION OF COMPOSITE FACIAL DEFECTS - THE COMBINED APPLICATIONOF MULTIPLE RECONSTRUCTIVE MODALITIES

      Canadian journal of surgery


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 31/10/20 alle ore 04:01:41