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

Brain & development (Tokyo. 1979), 2005-11, Vol.27, p.S8-S13

2005

Volltextzugriff (PDF)

Predictive value of the early clinical signs in Rett disorder

Brain & development (Tokyo. 1979), 2005-11, Vol.27, p.S20-S24

2005

Volltextzugriff (PDF)

Rapid Deployment of Whole Slide Imaging for Primary Diagnosis in Surgical Pathology at Stanford Medicine: Responding to Challenges of the COVID-19 Pandemic

Archives of pathology & laboratory medicine (1976), 2023-03, Vol.147 (3), p.359-367

2023

Volltextzugriff (PDF)

Reflections on the constraints and opportunities in therapy in Rett syndrome

TheScientificWorld, 2006-08, Vol.6, p.992-997

Kerr, Alison M

2006

Volltextzugriff (PDF)

Guidelines for reporting clinical features in cases with MECP2 mutations

Brain & development (Tokyo. 1979), 2001-07, Vol.23 (4), p.208-211

2001

Volltextzugriff (PDF)

Is the early development of girls with rett disorder really normal?

Pediatric research, 2005-05, Vol.57 (5), p.696-700

2005

Volltextzugriff (PDF)

NTNG1 mutations are a rare cause of Rett syndrome

American journal of medical genetics. Part A, 2006-04, Vol.140A (7), p.691-694

2006

Volltextzugriff (PDF)

Mind and brain in Rett disorder

Brain & development (Tokyo. 1979), 2001-12, Vol.23, p.S44-S49

2001

Volltextzugriff (PDF)

Kinematic and Kinetic Gait Characteristics of Normal Children Walking at a Range of Clinically Relevant Speeds

Journal of pediatric orthopaedics, 2002-11, Vol.22 (6), p.800-806

2002

Volltextzugriff (PDF)

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

European journal of human genetics : EJHG, 2005-10, Vol.13 (10), p.1121-1130

2005

Volltextzugriff (PDF)

Results of Surgery for Scoliosis in Rett Syndrome

Journal of child neurology, 2003-10, Vol.18 (10), p.703-708

2003

Volltextzugriff (PDF)

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

Journal of applied research in intellectual disabilities, 2005-09, Vol.18 (3), p.201-215

2005

Volltextzugriff (PDF)

Recent insights into hyperventilation from the study of Rett syndrome

Archives of disease in childhood, 1999-04, Vol.80 (4), p.384-387

1999

Volltextzugriff (PDF)

The mid-point of passive hip rotation range is an indicator of hip rotation in gait in cerebral palsy

Gait & posture, 2003-02, Vol.17 (1), p.88-91

2003

Volltextzugriff (PDF)

Rapid Deployment of Whole Slide Imaging for Primary Diagnosis in Surgical Pathology at Stanford Medicine

Archives of pathology & laboratory medicine (1976), 2023-03, Vol.147 (3), p.359-367

2023

Volltextzugriff (PDF)

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

European journal of paediatric neurology, 1998, Vol.2 (3), p.127-135

1998

Volltextzugriff (PDF)

Abnormalities in urinary pterin levels in Rett syndrome

European journal of paediatric neurology, 2000, Vol.4 (5), p.211-217

2000

Volltextzugriff (PDF)

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

Journal of child psychology and psychiatry, 2002-03, Vol.43 (3), p.277-287

Kerr, Alison

2002

Volltextzugriff (PDF)

Review article: Breaking new ground with Rett syndrome

Journal of intellectual disability research, 2003-11, Vol.47 (8), p.580-587

2003

Volltextzugriff (PDF)

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

Brain & development (Tokyo. 1979), 1987, Vol.9 (5), p.487-490

1987

Volltextzugriff (PDF)

Kinematic and Kinetic Gait Characteristics of Normal Children Walking at a Range of Clinically Relevant Speeds

Journal of pediatric orthopaedics, 2002-11, Vol.22 (6), p.800-806

2002

Volltextzugriff (PDF)

Mind and brain in Rett disorder

Brain & development (Tokyo. 1979), 2001, Vol.23, p.S44-S49

2001

Volltextzugriff (PDF)

Dysmorphic feet in rett syndrome: Genetic or developmental marker

Pediatric neurology, 1994-09, Vol.11 (2), p.135-135

1994

Volltextzugriff (PDF)

Letters to the Editor

Behavioural neurology, 1991, Vol.4 (3), p.203-205

1991

Volltextzugriff (PDF)

Guidelines for reporting clinical features in cases with MECP2 mutations

Brain & development (Tokyo. 1979), 2001, Vol.23 (4), p.208-211

2001

Volltextzugriff (PDF)

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

Predictive value of the early clinical signs in Rett disorder

Rapid Deployment of Whole Slide Imaging for Primary Diagnosis in Surgical Pathology at Stanford Medicine: Responding to Challenges of the COVID-19 Pandemic

Reflections on the constraints and opportunities in therapy in Rett syndrome

Guidelines for reporting clinical features in cases with MECP2 mutations

Is the early development of girls with rett disorder really normal?

NTNG1 mutations are a rare cause of Rett syndrome

Mind and brain in Rett disorder

Kinematic and Kinetic Gait Characteristics of Normal Children Walking at a Range of Clinically Relevant Speeds

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

Results of Surgery for Scoliosis in Rett Syndrome

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

Recent insights into hyperventilation from the study of Rett syndrome

The mid-point of passive hip rotation range is an indicator of hip rotation in gait in cerebral palsy

Rapid Deployment of Whole Slide Imaging for Primary Diagnosis in Surgical Pathology at Stanford Medicine

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

Abnormalities in urinary pterin levels in Rett syndrome

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

Review article: Breaking new ground with Rett syndrome

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

Kinematic and Kinetic Gait Characteristics of Normal Children Walking at a Range of Clinically Relevant Speeds

Mind and brain in Rett disorder

Dysmorphic feet in rett syndrome: Genetic or developmental marker

Letters to the Editor

Guidelines for reporting clinical features in cases with MECP2 mutations

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