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Dive into the research topics where Francis Mastaglia is active.

Publication


Featured researches published by Francis Mastaglia.


Neurogenetics | 1999

The α-synuclein gene is not a major risk factor in familial Parkinson disease [2]

William K. Scott; Larry H. Yamaoka; Jeffrey M. Stajich; Burton L. Scott; J. M. Vance; A. D. Roses; Margaret A. Pericak-Vance; R.L. Watts; M. Nance; J. Hubble; W. Koller; M.B. Stern; A. Colcher; F.H.Jr. Allen; B.C. Hiner; J. Jankovic; W. Ondo; Nigel Laing; Francis Mastaglia; C. Goetz; E. Pappert; Gary W. Small; D. Masterman; Jonathan L. Haines


Archive | 2001

Complete genomic screen in Parkinson Disease

William K. Scott; Nance; Ray L. Watts; Jean Hubble; William C. Koller; Kelly E. Lyons; Rajesh Pahwa; Matthew B. Stern; Amy Colcher; Bradley C. Hiner; Joseph Jankovic; William G. Ondo; Fred H. Allen; Christopher G. Goetz; Gary W. Small; Donna Masterman; Francis Mastaglia; Nigel G. Laing; Jeffrey M. Stajich; Brandon D. Slotterbeck; Michael W. Booze; Robert C. Ribble; Evadnie Rampersaud; Sandra G. West; Rachel A. Gibson; Lefkos T. Middleton; A. D. Roses; Jonathan L. Haines; Burton L. Scott; J. M. Vance


Autosomal dominant distal myopathy linkage on Chromosome 14 | 1994

Autosomal dominant distal myopathy linkage on Chromosome 14

C. Meredith; B.A. Laing; S.D. Wilton; Francis Mastaglia; Peter Robbins; H. Kozman; K. Honeyman; S.M. Dorosz; Byron Kakulas; Nigel G. Laing


Hereditary distal myopathy | 1993

Hereditary distal myopathy

B.A. Laing; C. Meredith; Francis Mastaglia; Nigel G. Laing; Peter Robbins


Analysis of the myelin protein zero (Po) in a large West Australian family with dominant, intermediate HMSN | 1998

Analysis of the myelin protein zero (Po) in a large West Australian family with dominant, intermediate HMSN

Kristen J. Nowak; Rick Stell; Francis Mastaglia; Beverley A. Phillips; V. Fabian; S.M. Dorosz; Nigel G. Laing


Analysis of the myelin protein zero (Po) gene in a large Western Australian family with dominant, intermediate HMSM | 1998

Analysis of the myelin protein zero (Po) gene in a large Western Australian family with dominant, intermediate HMSM

Kristen J. Nowak; Rick Stell; Francis Mastaglia; Beverley A. Phillips; V. Fabian; S.M. Dorosz; Nigel G. Laing


Dominantly inherited proximal myotonic myopathy and leucoencephalopathy in a family with an incidental CLCN1 mutation | 1997

Dominantly inherited proximal myotonic myopathy and leucoencephalopathy in a family with an incidental CLCN1 mutation

Francis Mastaglia; N. Harker; Beverley A. Phillips; Timothy Day; G. Hankey; V. Fabian; Nigel G. Laing


Dominantly Inherited Proximal Myotonic Myopathy and Leucoencephalopathy in a Family with an Incidental CLCNI Mutation | 1997

Dominantly Inherited Proximal Myotonic Myopathy and Leucoencephalopathy in a Family with an Incidental CLCNI Mutation

Francis Mastaglia; N. Harker; Beverley A. Phillips; Timothy Day; G. Hankey; V. Fabian; Nigel G. Laing


The Clinical Biochemist Reviews | 1993

An autosomal dominant distal myopathy - preliminary linkage to chromosome 14

Nigel G. Laing; B.A. Laing; C. Meredith; S.D. Wilton; Francis Mastaglia; Peter D. Robbins; K. Honeyman; S.M. Dorosz; Byron Kakulas


Molecular genetics: another diagnostic weapon | 1992

Molecular genetics: another diagnostic weapon

Nigel G. Laing; S.D. Wilton; D.C. Chandfler; Rick Stell; Francis Mastaglia

Collaboration


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B.A. Laing

University of Western Australia

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C. Meredith

Edith Cowan University

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Peter Robbins

Sir Charles Gairdner Hospital

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Rick Stell

Sir Charles Gairdner Hospital

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Byron Kakulas

University of Western Australia

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K. Honeyman

University of Western Australia

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Timothy Day

Royal Melbourne Hospital

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