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Results: 1-25 | 26-30
Results: 1-25/30
THE NATURAL-HISTORY OF NEUROFIBROMATOSIS-2 IN 31 AFFECTED CHILDREN
Authors: MACCOLLIN M BOVE C KLUWE L OJEMANN R MAUTNER VF
Citation: M. Maccollin et al., THE NATURAL-HISTORY OF NEUROFIBROMATOSIS-2 IN 31 AFFECTED CHILDREN, Annals of neurology, 44(3), 1998, pp. 45-45
PHENOTYPIC VARIABILITY ASSOCIATED WITH 14 SPLICE-SITE MUTATIONS IN THE NF2 GENE
Authors: KLUWE L MACCOLLIN M TATAGIBA M THOMAS S HAZIM W HAASE W MAUTNER VF
Citation: L. Kluwe et al., PHENOTYPIC VARIABILITY ASSOCIATED WITH 14 SPLICE-SITE MUTATIONS IN THE NF2 GENE, American journal of medical genetics, 77(3), 1998, pp. 228-233
THE EFFECT OF CHANGES IN HEARING STATUS ON SPEECH SOUND LEVEL AND SPEECH BREATHING - A STUDY CONDUCTED WITH COCHLEAR IMPLANT USERS AND NF-2PATIENTS
Authors: LANE H PERKELL J WOZNIAK J MANZELLA J GUIOD P MATTHIES M MACCOLLIN M VICK J
Citation: H. Lane et al., THE EFFECT OF CHANGES IN HEARING STATUS ON SPEECH SOUND LEVEL AND SPEECH BREATHING - A STUDY CONDUCTED WITH COCHLEAR IMPLANT USERS AND NF-2PATIENTS, The Journal of the Acoustical Society of America, 104(5), 1998, pp. 3059-3069
SCHWANNOMATOSIS RESULTING FROM SOMATIC MOSAICISM OF THE NF2 GENE
Authors: MACCOLLIN M KRONN D DAVIS K JONES D JACOBY LB
Citation: M. Maccollin et al., SCHWANNOMATOSIS RESULTING FROM SOMATIC MOSAICISM OF THE NF2 GENE, Annals of neurology, 42(3), 1997, pp. 50-50
THE NATURAL-HISTORY OF EPENDYMOMA IN PATIENTS WITH NEUROFIBROMATOSIS-2
Authors: JONES RM MACCOLLIN M
Citation: Rm. Jones et M. Maccollin, THE NATURAL-HISTORY OF EPENDYMOMA IN PATIENTS WITH NEUROFIBROMATOSIS-2, Neurology, 48(3), 1997, pp. 1030-1030
SOMATIC MOSAICISM OF THE NEUROFIBROMATOSIS-2 TUMOR-SUPPRESSOR GENE
Authors: MACCOLLIN M JACOBY LB JONES D OJEMANN R FEIT H GUSELLA J
Citation: M. Maccollin et al., SOMATIC MOSAICISM OF THE NEUROFIBROMATOSIS-2 TUMOR-SUPPRESSOR GENE, Neurology, 48(3), 1997, pp. 6095-6095
SPINAL SCHWANNOMATOSIS - REPLY
Authors: MACCOLLIN M JACOBY L WOODFIN W SHORT MP
Citation: M. Maccollin et al., SPINAL SCHWANNOMATOSIS - REPLY, Neurology, 48(3), 1997, pp. 787-788
MOLECULAR ANALYSIS OF THE NF2 TUMOR-SUPPRESSOR GENE IN SCHWANNOMATOSIS
Authors: JACOBY LB JONES D DAVIS K KRONN D SHORT MP GUSELLA J MACCOLLIN M
Citation: Lb. Jacoby et al., MOLECULAR ANALYSIS OF THE NF2 TUMOR-SUPPRESSOR GENE IN SCHWANNOMATOSIS, American journal of human genetics, 61(6), 1997, pp. 1293-1302
FREQUENCY AND DISTRIBUTION OF NF2 MUTATIONS IN SCHWANNOMAS
Authors: JACOBY LB MACCOLLIN M BARONE R RAMESH V GUSELLA JF
Citation: Lb. Jacoby et al., FREQUENCY AND DISTRIBUTION OF NF2 MUTATIONS IN SCHWANNOMAS, Genes, chromosomes & cancer, 17(1), 1996, pp. 45-55
NEUROFIBROMATOSIS-2 - LOSS OF MERLIN PROTECTIVE SPELL
Authors: GUSELLA JF RAMESH V MACCOLLIN M JACOBY LB
Citation: Jf. Gusella et al., NEUROFIBROMATOSIS-2 - LOSS OF MERLIN PROTECTIVE SPELL, Current opinion in genetics & development, 6(1), 1996, pp. 87-92
A POINT MUTATION ASSOCIATED WITH A SEVERE PHENOTYPE OF NEUROFIBROMATOSIS-2
Authors: MACCOLLIN M BRAVERMAN N VISKOCHIL D RUTTLEDGE M DAVIS K OJEMANN R GUSELLA J PARRY DM
Citation: M. Maccollin et al., A POINT MUTATION ASSOCIATED WITH A SEVERE PHENOTYPE OF NEUROFIBROMATOSIS-2, Annals of neurology, 40(3), 1996, pp. 440-445
THE PARENTAL ORIGIN OF NEW MUTATION IN NEUROFIBROMATOSIS-2
Authors: MACCOLLIN M DAVIS K PARRY D BASER M GUSELLA J
Citation: M. Maccollin et al., THE PARENTAL ORIGIN OF NEW MUTATION IN NEUROFIBROMATOSIS-2, Annals of neurology, 40(2), 1996, pp. 12-12
SCHWANNOMATOSIS - A CLINICAL AND PATHOLOGICAL-STUDY
Authors: MACCOLLIN M WOODFIN W KRONN D SHORT MP
Citation: M. Maccollin et al., SCHWANNOMATOSIS - A CLINICAL AND PATHOLOGICAL-STUDY, Neurology, 46(4), 1996, pp. 1072-1079
CHARACTERIZATION AND EXPRESSION OF THE HUMAN A2A ADENOSINE RECEPTOR GENE
Authors: PETERFREUND RA MACCOLLIN M GUSELLA J FINK JS
Citation: Ra. Peterfreund et al., CHARACTERIZATION AND EXPRESSION OF THE HUMAN A2A ADENOSINE RECEPTOR GENE, Journal of neurochemistry, 66(1), 1996, pp. 362-368
TYPE OF MUTATION IN THE NEUROFIBROMATOSIS TYPE-2 GENE (NF2) FREQUENTLY DETERMINES SEVERITY OF DISEASE
Authors: RUTTLEDGE MH ANDERMANN AA PHELAN CM CLAUDIO JO HAN FY CHRETIEN N RANGARATNAM S MACCOLLIN M SHORT P PARRY D MICHELS V RICCARDI VM WEKSBERG R KITAMURA K BRADBURN JM HALL BD PROPPING P ROULEAU GA
Citation: Mh. Ruttledge et al., TYPE OF MUTATION IN THE NEUROFIBROMATOSIS TYPE-2 GENE (NF2) FREQUENTLY DETERMINES SEVERITY OF DISEASE, American journal of human genetics, 59(2), 1996, pp. 331-342
MOLECULAR-GENETIC SCREENING FOR CHILDREN AT RISK OF NEUROFIBROMATOSIS.2.
Authors: HARSH GR MACCOLLIN M MCKENNA MJ NADOL JB OJEMANN R SHORT MP
Citation: Gr. Harsh et al., MOLECULAR-GENETIC SCREENING FOR CHILDREN AT RISK OF NEUROFIBROMATOSIS.2., Archives of otolaryngology, head & neck surgery, 121(5), 1995, pp. 590-591
CNS YOUNG INVESTIGATOR AWARD LECTURE - MOLECULAR ANALYSIS OF THE NEUROFIBROMATOSIS-2 TUMOR-SUPPRESSOR
Authors: MACCOLLIN M
Citation: M. Maccollin, CNS YOUNG INVESTIGATOR AWARD LECTURE - MOLECULAR ANALYSIS OF THE NEUROFIBROMATOSIS-2 TUMOR-SUPPRESSOR, Brain & development, 17(4), 1995, pp. 231-238
IDENTICAL INACTIVATING MUTATION IN 3 CHILDREN WITH NEUROFIBROMATOSIS TYPE-2
Authors: MACCOLLIN M BRAVERMAN N SIFFERT J HOFMAN K GUSELLA J PARRY D
Citation: M. Maccollin et al., IDENTICAL INACTIVATING MUTATION IN 3 CHILDREN WITH NEUROFIBROMATOSIS TYPE-2, Annals of neurology, 38(3), 1995, pp. 554-554
MOLECULAR ANALYSIS OF THE MYELIN BASIC-PROTEIN IN LEUKODYSTROPHY
Authors: MACCOLLIN M DALEY M PULASKI K GUSELLA J NATOWICZ M
Citation: M. Maccollin et al., MOLECULAR ANALYSIS OF THE MYELIN BASIC-PROTEIN IN LEUKODYSTROPHY, Neurology, 45(4), 1995, pp. 402-402
SEARCH FOR CORRELATIONS BETWEEN CLINICAL SUBTYPES AND GENOTYPES IN NEUROFIBROMATOSIS-2 (NF2)
Authors: PARRY DM MACCOLLIN M PULASKI K ELDRIDGE R FGUSELLA J
Citation: Dm. Parry et al., SEARCH FOR CORRELATIONS BETWEEN CLINICAL SUBTYPES AND GENOTYPES IN NEUROFIBROMATOSIS-2 (NF2), Neurology, 45(4), 1995, pp. 440-441
ADVISABILITY OF TESTING CHILDREN AND ADOLESCENTS PRESYMTOMATICALLY FOR NFII - FAMILIES AND NURSES PERCEPTIONS
Authors: BOVE C MACCOLLIN M SHORT MP ADAMS D
Citation: C. Bove et al., ADVISABILITY OF TESTING CHILDREN AND ADOLESCENTS PRESYMTOMATICALLY FOR NFII - FAMILIES AND NURSES PERCEPTIONS, American journal of human genetics, 57(4), 1995, pp. 2017-2017
THE MURINE NF2 HOMOLOG ENCODES A HIGHLY CONSERVED MERLIN PROTEIN WITHALTERNATIVE FORMS
Authors: HAASE VH TROFATTER JA MACCOLLIN M TARTTELIN E GUSELLA JF RAMESH V
Citation: Vh. Haase et al., THE MURINE NF2 HOMOLOG ENCODES A HIGHLY CONSERVED MERLIN PROTEIN WITHALTERNATIVE FORMS, Human molecular genetics, 3(3), 1994, pp. 407-411
EXON SCANNING FOR MUTATION OF THE NF2 GENE IN SCHWANNOMAS
Authors: JACOBY LB MACCOLLIN M LOUIS DN MOHNEY T RUBIO MP PULASKI K TROFATTER JA KLEY N SEIZINGER B RAMESH V GUSELLA JF
Citation: Lb. Jacoby et al., EXON SCANNING FOR MUTATION OF THE NF2 GENE IN SCHWANNOMAS, Human molecular genetics, 3(3), 1994, pp. 413-419
MAPPING OF A HUMAN-A2A ADENOSINE RECEPTOR (ADORA2) TO CHROMOSOME-22
Authors: MACCOLLIN M PETERFREUND R MACDONALD M FINK JS GUSELLA J
Citation: M. Maccollin et al., MAPPING OF A HUMAN-A2A ADENOSINE RECEPTOR (ADORA2) TO CHROMOSOME-22, Genomics, 20(2), 1994, pp. 332-333
THE MERLIN TUMOR-SUPPRESSOR IN NEUROFIBROMATOSIS-2
Authors: JACOBY LB MACCOLLIN M LOUIS DN TROFATTER JA KLEY N SEIZINGER B RAMESH V GUSELLA JF
Citation: Lb. Jacoby et al., THE MERLIN TUMOR-SUPPRESSOR IN NEUROFIBROMATOSIS-2, Journal of cellular biochemistry, 1994, pp. 163-163
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