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O.077 Risk factors, prevention and treatment of CSF fistulas after vestibular schwannoma surgery

Clinical neurology and neurosurgery, 2008-01, Vol.110 (S1), p.S21-S21

2008

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O.022 Anatomical study of the quadrigeminal cistern in the living with three-dimensional MR cisternography

Clinical neurology and neurosurgery, 2008-01, Vol.110 (S1), p.S6-S7

2008

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4CPS-339 Intrathecal administration of baclofen for the reduction of spasticity

European journal of hospital pharmacy. Science and practice, 2021-03, Vol.28 (Suppl 1), p.A84-A84

2021

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The Intrasacral Meningocele: A Clinical Study

Rivista di neuroradiologia, 2005-12, Vol.18 (5-6), p.617-620

2005

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Tubulin nitration in human gliomas

Neuroscience letters, 2006-02, Vol.394 (1), p.57-62

2006

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Partial monosomy for chromosome 22 in a patient with del(22)(pter----q13.1::q13.33----qter)

Journal of medical genetics, 1990-09, Vol.27 (9), p.588-589

1990

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Three cases of partial trisomy 7q owing to rare structural rearrangements of chromosome 7

Journal of medical genetics, 1990-02, Vol.27 (2), p.109-113

1990

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9-Cis retinoic acid is a direct hepatocyte mitogen in rats

Life sciences (1973), 1996, Vol.58 (11), p.PL211-PL216

1996

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Bloom syndrome and maternal uniparental disomy for chromosome 15

American journal of human genetics, 1994-07, Vol.55 (1), p.74-80

1994

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Trisomy 18 with karyotype 47,XX,-18+i psu dic(18p)

Journal of medical genetics, 1992-07, Vol.29 (7), p.513-513

1992

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A complex structural rearrangement of chromosome 4 in a woman without phenotypic features of Wolf-Hirschhorn syndrome

Clinical genetics, 1985-08, Vol.28 (2), p.166-172

1985

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Tethered cord syndrome

Journal of neurosurgical sciences, 2005-12, Vol.49 (4), p.131

2005

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Familial distal trisomy 8(q24.13----qter)

Journal of medical genetics, 1989-02, Vol.26 (2), p.133-138

1989

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Partial trisomy for 2q in a patient with dir dup(2) (q33.1q35)

Journal of medical genetics, 1994-08, Vol.31 (8), p.652-653

1994

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Late replication studies and esterase D levels in a case of unbalanced X;autosome translocation, 46,X,t(X;13)(q27;q12)

Journal of medical genetics, 1988-10, Vol.25 (10), p.716-718

1988

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Two cases of ring chromosome 11

Journal of medical genetics, 1983-10, Vol.20 (5), p.380-382

1983

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Studies on three rare fragile sites: 2q13, 12q13, and 17p12 segregating in one family

Human genetics, 1986-06, Vol.73 (2), p.164-170

1986

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Discovery of an inherited bisatellited metacentric microchromosome in amniotic cell culture

Clinical genetics, 1979-09, Vol.16 (3), p.183-190

1979

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Direct intrachromosomal duplication of 16q and heritable fragile site fra (10) (q25) in the same patient

American journal of medical genetics, 1984-11, Vol.19 (3), p.507-513

1984

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Partial monosomy 12p13.1----13.3

Journal of medical genetics, 1987-07, Vol.24 (7), p.434-436

1987

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A complex chromosome rearrangement forms the BCR-ABL fusion gene in leukemic cells with a normal karyotype

Genes chromosomes & cancer, 1991-07, Vol.3 (4), p.263-271

1991

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Two pericentric inversions, inv(2)(p11q13) and inv(5)(p13q13), in a patient referred for psychiatric problems

Journal of medical genetics, 1982-04, Vol.19 (2), p.153-155

1982

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Three unrelated cases of accessory bisatellited microchromosomes in New Zealand

New Zealand medical journal, 1981-08, Vol.94 (689), p.90

1981

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t(2;14)(q23;q32.3) as the sole abnormality in a patient with acute nonlymphocytic leukemia (FAB-M4)

Cancer genetics and cytogenetics, 1990-09, Vol.48 (2), p.255-257

1990

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Familial paracentric inversion of 1p

American journal of medical genetics, 1983-04, Vol.14 (4), p.629-634

1983

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O.077 Risk factors, prevention and treatment of CSF fistulas after vestibular schwannoma surgery

O.022 Anatomical study of the quadrigeminal cistern in the living with three-dimensional MR cisternography

4CPS-339 Intrathecal administration of baclofen for the reduction of spasticity

The Intrasacral Meningocele: A Clinical Study

Tubulin nitration in human gliomas

Partial monosomy for chromosome 22 in a patient with del(22)(pter----q13.1::q13.33----qter)

Three cases of partial trisomy 7q owing to rare structural rearrangements of chromosome 7

9-Cis retinoic acid is a direct hepatocyte mitogen in rats

Bloom syndrome and maternal uniparental disomy for chromosome 15

Trisomy 18 with karyotype 47,XX,-18+i psu dic(18p)

A complex structural rearrangement of chromosome 4 in a woman without phenotypic features of Wolf-Hirschhorn syndrome

Tethered cord syndrome

Familial distal trisomy 8(q24.13----qter)

Partial trisomy for 2q in a patient with dir dup(2) (q33.1q35)

Late replication studies and esterase D levels in a case of unbalanced X;autosome translocation, 46,X,t(X;13)(q27;q12)

Two cases of ring chromosome 11

Studies on three rare fragile sites: 2q13, 12q13, and 17p12 segregating in one family

Discovery of an inherited bisatellited metacentric microchromosome in amniotic cell culture

Direct intrachromosomal duplication of 16q and heritable fragile site fra (10) (q25) in the same patient

Partial monosomy 12p13.1----13.3

A complex chromosome rearrangement forms the BCR-ABL fusion gene in leukemic cells with a normal karyotype

Two pericentric inversions, inv(2)(p11q13) and inv(5)(p13q13), in a patient referred for psychiatric problems

Three unrelated cases of accessory bisatellited microchromosomes in New Zealand

t(2;14)(q23;q32.3) as the sole abnormality in a patient with acute nonlymphocytic leukemia (FAB-M4)

Familial paracentric inversion of 1p

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