A. Kerr

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Is the Early Development of Girls with Rett Disorder Really Normal?

C. Einspieler, H. Prechtl, A. Kerr, 2005, Pediatric Research.

Reflections on the Constraints and Opportunities in Therapy in Rett Syndrome

A. Kerr, 2006, TheScientificWorldJournal.

Feeding ability in Rett syndrome

A. Kerr, R. Ellis, R. Morton, 1997, Developmental medicine and child neurology.

Workshop on Autonomic Function in Rett Syndrome. Swedish Rett Center Frösön, Sweden, May 1998.

A. Kerr, I. Engerström, 1998, Brain & development.

Early onset seizures and Rett-like features associated with mutations in CDKL5

J. Gécz, D. Cooper, A. Clarke, 2005, European Journal of Human Genetics.

Predictive value of the early clinical signs in Rett disorder

R. Prescott, A. Kerr, 2005, Brain and Development.

Report on the Rett Syndrome Workshop: Glasgow, Scotland, 24-25 May 1986

A. Kerr, 2008 .

Immaturity of medullary cardiorespiratory neurones leading to inappropriate autonomic reactions as a likely cause of sudden death in Rett’s syndrome

G. Jamal, S. Hansen, A. Kerr, 1997, Archives of disease in childhood.

Rett syndrome: analysis of deaths in the British survey.

R. Prescott, A. Kerr, D. Armstrong, 1997, European child & adolescent psychiatry.

NTNG1 mutations are a rare cause of Rett syndrome

A. Clarke, D. Pilz, J. Christodoulou, 2006, American journal of medical genetics. Part A.

Rett's syndrome in the west of Scotland.

J. Stephenson, A. Kerr, 1985, British medical journal.

Results of Surgery for Scoliosis in Rett Syndrome

R. Prescott, A. Kerr, P. Webb, 2003, Journal of child neurology.

Abnormalities in urinary pterin levels in Rett syndrome.

H. Pall, A. Kerr, S. Messahel, 2000, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Gross rearrangements of the MECP2 gene are found in both classical and atypical Rett syndrome patients

W. Reardon, D. Cooper, Y. Crow, 2005, Journal of Medical Genetics.

Dimensional phenotypic analysis and functional categorisation of mutations reveal novel genotype–phenotype associations in Rett syndrome

R. Hastings, T. Charman, A. Clarke, 2005, European Journal of Human Genetics.

Increased skewing of X chromosome inactivation in Rett syndrome patients and their mothers

M. Schwartz, G. Knudsen, M. Bailey, 2006, European Journal of Human Genetics.

Rett syndrome: critical examination of clinical features, serial EEG and video-monitoring in understanding and management.

A. Kerr, R. Cooper, P. Amos, 1998, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

p.R270X MECP2 mutation and mortality in Rett syndrome

J. Christodoulou, H. Leonard, D. Ravine, 2005, European Journal of Human Genetics.

MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved region

S. Dhanjal, M. D'Esposito, M. D'urso, 2001, Brain and Development.

Medical needs of people with intellectual disability require regular reassessment, and the provision of client- and carer-held reports.

D. McCulloch, A. Kerr, S. Wallace, 2003, Journal of intellectual disability research : JIDR.

Mind and brain in Rett disorder

P. Belichenko, A. Kerr, T. Woodcock, 2001, Brain and Development.

Early Clinical Signs in the Rett Disorder

A. Kerr, Alison Kerr, 1995, Neuropediatrics.

Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location.

D. Cooper, M. Krawczak, A. Clarke, 2000, Human molecular genetics.

Guidelines for reporting clinical features in cases with MECP2 mutations

Masaya Segawa, Yushiro Yamashita, Uta Francke, 2001, Brain and Development.

Characterisation of breathing and associated central autonomic dysfunction in the Rett disorder

G. Jamal, S. Hansen, A. Kerr, 2001, Archives of disease in childhood.

Recent insights into hyperventilation from the study of Rett syndrome

A. Kerr, P. Julu, 1999, Archives of disease in childhood.

Hyperventilation in the awake state: potentially treatable component of Rett syndrome.

D. Southall, J. Stephenson, A. Kerr, 1988, Archives of disease in childhood.

Functional evidence of brain stem immaturity in Rett syndrome.

G. Jamal, S. Hansen, A. Kerr, 1997, European child & adolescent psychiatry.

The hands, and the mind, pre- and post-regression in rett syndrome

J. Stephenson, A. Kerr, J. Montague, 1987, Brain and Development.

Variation in exon 1 coding region and promoter of MECP2 in Rett syndrome and controls

A. Clarke, H. Archer, A. Kerr, 2005, European Journal of Human Genetics.

Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females

S. Dhanjal, M. D'Esposito, M. D'urso, 2001, Journal of Molecular Medicine.

Review article: breaking new ground with Rett syndrome.

D. Ravine, A. Kerr, D. Ravine, 2003, Journal of intellectual disability research : JIDR.

, patients in both classical and atypical Rett syndrome gene are foundMECP 2 Gross rearrangements

W. Reardon, D. Cooper, Y. Crow, 2006 .

, in both classical and atypical Rett Syndrome Gross rearrangements of the MECP 2 gene are found

W. Reardon, D. Cooper, Y. Crow, 2005 .

Large genomic rearrangements in MECP2

M. Schwartz, O. Skjeldal, M. Hultén, 2005, Human mutation.

Annotation: Rett syndrome: recent progress and implications for research and clinical practice.

A. Kerr, Alison Kerr, 2002, Journal of child psychology and psychiatry, and allied disciplines.

Recent developments in Rett syndrome research

A. Kerr, 2001 .

People with MECP2 mutation-positive Rett disorder who converse.

R. Prescott, J. Evans, F. Gibbon, 2006, Journal of intellectual disability research : JIDR.

Nurse recognition of early deviation in development in home videos of infants with Rett disorder.

A. Kerr, B. Burford, H. A. Macleod, 2003, Journal of intellectual disability research : JIDR.

Towards a full life with Rett disorder

A. Kerr, B. Burford, Bronwen Burford, 2001, Pediatric rehabilitation.

Rett syndrome and the 4th metatarsal.

A. Kerr, J. Mitchell, P. Robertson, 1993, Archives of disease in childhood.

Two cases of ring chromosome 11.

A. Kerr, C. Chapman, D. Romain, 1983, Journal of medical genetics.

Mutation analysis in the MECP2 gene and genetic counselling for Rett syndrome

F. Hanefeld, A. Clarke, J. Christodoulou, 2003, Journal of medical genetics.

Acetazolamide in prevention of acute mountain sickness: a double-blind controlled cross-over study.

R. Prescott, A. Kerr, I. Mcintosh, 1981, British medical journal.

Abnormal general movements in girls with Rett disorder: The first four months of life

C. Einspieler, H. Prechtl, A. Kerr, 2005, Brain and Development.

Correlation of electroencephalogram, respiration and movement in the Rett syndrome

D. Southall, M. Samuels, J. Stephenson, 1990, Brain and Development.

Sleep Disturbance in Children with Rett Syndrome: A Qualitative Investigation of the Parental Experience

C. Espie, A. Kerr, A. McDougall, 2005 .

A review of the respiratory disorder in the Rett syndrome.

A. Kerr, 1992, Brain & development.

EMOTIONAL AND BEHAVIOURAL ASPECTS OF RETT SYNDROME

V. Krishnan, A. Kerr, J. Corbett, 1993, Developmental medicine and child neurology.

A study of the natural history of Rett syndrome in 23 girls.

J. Stephenson, A. Kerr, 1986, American journal of medical genetics. Supplement.

Rett Syndrome: From Gene to Gesture

Alison Kerr, John Corbett, A. Kerr, 1994, Journal of the Royal Society of Medicine.

Neurophysiological observations on corticospinal projections to the upper limb in subjects with Rett syndrome.

S. Miller, J. Eyre, V. Ramesh, 1990, Journal of neurology, neurosurgery, and psychiatry.

Motion analysis of stereotyped hand movements in Rett syndrome.

M. L. van der Linden, A. Kerr, G. Arrowsmith, 2003, Journal of intellectual disability research : JIDR.

Rett disorder and the developing brain

A. Kerr, I. Engerström, 2001 .

Short fourth toes in Rett syndrome: a biological indicator.

A. Kerr, J. Mitchell, P. Robertson, 1995, Neuropediatrics.

Molecular genetic studies in familial Rett syndrome

M. Owen, K. Davies, N. Williams, 1997 .

Hyperventilation intheawakestate: potentially treatable componentofRettsyndrome

D. Southall, A. Kerr, M. H. Lang, 1988 .