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Results:
1-16
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Results: 16
Authors:
Bruder, CEG
Hirvela, C
Tapia-Paez, I
Fransson, I
Segraves, R
Hamilton, G
Zhang, XX
Evans, DG
Wallace, AJ
Baser, ME
Zucman-Rossi, J
Hergersberg, M
Boltshauser, E
Papi, L
Rouleau, GA
Poptodorov, G
Jordanova, A
Rask-Andersen, H
Kluwe, L
Mautner, V
Sainio, M
Hung, G
Mathiesen, T
Moller, C
Pulst, SM
Harder, H
Heiberg, A
Honda, M
Miimura, M
Sahlen, S
Blennow, E
Albertson, DG
Pinkel, D
Dumanski, JP
Citation: Ceg. Bruder et al., High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH, HUM MOL GEN, 10(3), 2001, pp. 271-282
Authors:
Toelle, SP
Valsangiacomo, E
Boltshauser, E
Citation: Sp. Toelle et al., Trichothiodystrophy with severe cardiac and neurological involvement in two sisters, EUR J PED, 160(12), 2001, pp. 728-731
Authors:
Boltshauser, E
Citation: E. Boltshauser, Cerebellar imaging - an important signpost in paediatric neurology, CHILD NERV, 17(4-5), 2001, pp. 211-216
Authors:
Toelle, SP
Boltshauser, E
Citation: Sp. Toelle et E. Boltshauser, Long-term outcome in children with congenital unilateral facial nerve palsy, NEUROPEDIAT, 32(3), 2001, pp. 130-135
Authors:
Schneider, JF
Boltshauser, E
Neuhaus, TJ
Rauscher, C
Martin, E
Citation: Jf. Schneider et al., MRI and proton spectroscopy in Lowe syndrome, NEUROPEDIAT, 32(1), 2001, pp. 45-48
Authors:
Schmugge, M
Frischknecht, H
Yonekawa, Y
Baumgartner, RW
Boltshauser, E
Humbert, J
Citation: M. Schmugge et al., Stroke in hemoglobin (SD) sickle cell disease with moyamoya: successful hydroxyurea treatment after cerebrovascular bypass surgery, BLOOD, 97(7), 2001, pp. 2165-2167
Authors:
Schmugge, M
Boltshauser, E
Pluss, HJ
Niggli, FK
Citation: M. Schmugge et al., Long-term follow-up and residual sequelae after treatment for intracerebral germ-cell tumour in children and adolescents, ANN ONCOL, 11(5), 2000, pp. 527-533
Authors:
Huisman, TAGM
Brandner, S
Niggli, F
Betts, DR
Boltshauser, E
Martin, E
Citation: Tagm. Huisman et al., Malignant rhabdoid tumor of the brain: Quantitative H-1 MR-spectroscopy and cytogenetics, NEUROPEDIAT, 31(3), 2000, pp. 159-161
Authors:
Hafezi, F
Boltshauser, E
Landau, K
Citation: F. Hafezi et al., Pronounced physiological pupillary hippus, KLIN MONATS, 216(2), 2000, pp. 118-119
Authors:
Tan, P
Briner, J
Boltshauser, E
Davis, MR
Wilton, SD
North, K
Wallgren-Pettersson, C
Laing, NG
Citation: P. Tan et al., Homozygosity for a nonsense mutation in the alpha-tropomyosin slow gene TPM3 in a patient with severe infantile nemaline myopathy, NEUROMUSC D, 9(8), 1999, pp. 573-579
Authors:
Maria, BL
Boltshauser, E
Palmer, SC
Tran, TX
Citation: Bl. Maria et al., Clinical features and revised diagnostic criteria in Joubert syndrome, J CHILD NEU, 14(9), 1999, pp. 583-590
Authors:
Chance, PF
Cavalier, L
Satran, D
Pellegrino, JE
Boltshauser, E
Koening, M
Dobyns, WB
Citation: Pf. Chance et al., Clinical nosologic and genetic aspects of Joubert and related syndromes (vol 14, pg 660, 1999), J CHILD NEU, 14(12), 1999, pp. 823-823
Authors:
Huisman, TAGM
Wohlrab, G
Nadal, D
Boltshauser, E
Martin, E
Citation: Tagm. Huisman et al., Unusual presentations of neuroborreliosis (Lyme disease) in childhood, J COMPUT AS, 23(1), 1999, pp. 39-42
Authors:
Steinlin, M
Knecht, B
Konu, D
Martin, E
Boltshauser, E
Citation: M. Steinlin et al., Neonatal Escherichia coli meningitis: spinal adhesions as a late complication, EUR J PED, 158(12), 1999, pp. 968-970
Authors:
Steinlin, M
Styger, M
Boltshauser, E
Citation: M. Steinlin et al., Cognitive impairments in patients with congenital nonprogressive cerebellar ataxia, NEUROLOGY, 53(5), 1999, pp. 966-973
Authors:
Brodsky, MC
Landau, K
Wilson, RS
Boltshauser, E
Citation: Mc. Brodsky et al., Morning glory disc anomaly in neurofibromatosis type 2, ARCH OPHTH, 117(6), 1999, pp. 839-841
Risultati:
1-16
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