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Rett Syndrome
Known as:
disorder retts
, Rett Syndrome [Disease/Finding]
, Rett's Disorder
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An inherited neurological developmental disorder that is associated with X-LINKED INHERITANCE and may be lethal in utero to hemizygous males. The…
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National Institutes of Health
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Related topics
Related topics
40 relations
Ataxia, Truncal
Autism Spectrum Disorders
Autistic behavior
Bruxism
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Broader (6)
Brain Diseases
Congenital anomaly of brain
Congenital disease of brain
Hereditary Diseases
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Narrower (3)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
Rett Syndrome, Preserved Speech Variant
Rett Syndrome, Zappella Variant
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2006
Highly Cited
2006
Curriculum restructuring in Higher Education after the Bologna Process: a new pedagogic regime?
Berit Karseth
2006
Corpus ID: 54576582
By adopting the Bologna Process as the frame of reference this article discusses the ongoing policy of curriculum restructuring…
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Review
2005
Review
2005
Gametes and Embryo Epigenetic Reprogramming Affect Developmental Outcome: Implication for Assisted Reproductive Technologies
S. Jacob
,
K. Moley
Pediatric Research
2005
Corpus ID: 23522989
There is concern about the health of children who are conceived with the use assisted reproductive technologies (ART). In…
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Review
2003
Review
2003
An Overview of Research Advances in Road Traffic Trauma in China
Zhengguo Wang
,
Jianxin Jiang
Traffic Injury Prevention
2003
Corpus ID: 19432479
With rapid development of social economies, road traffic accidents (RTAs) have continued to increase, and have become the…
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Highly Cited
2001
Highly Cited
2001
Multicolor fluorescent in situ hybridization on post-mortem brain in schizophrenia as an approach for identification of low-level chromosomal aneuploidy in neuropsychiatric diseases
Y. Yurov
,
V. M. Vostrikov
,
S. Vorsanova
,
V. V. Monakhov
,
I. Iourov
Brain & development (Tokyo. )
2001
Corpus ID: 31105017
Highly Cited
2001
Highly Cited
2001
MECP2 truncating mutations cause histone H4 hyperacetylation in Rett syndrome.
Mimi Wan
,
K. Zhao
,
S. Lee
,
U. Francke
Human Molecular Genetics
2001
Corpus ID: 8802582
Rett syndrome (RTT) is a mostly sporadic disorder of developmental regression, with loss of speech and purposeful hand use…
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Review
1994
Review
1994
Rett Syndrome - Clinical and Biological Aspects
J. Stephenson
Archives of Disease in Childhood
1994
Corpus ID: 43316989
Large textbooks are not my best friend they are too heavy to carry, too intimidating to read, and I am too mindful of my own…
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Highly Cited
1987
Highly Cited
1987
Rett syndrome in Sweden
I. Witt‐Engerström
,
C. Gillberg
Journal of Autism and Developmental Disorders
1987
Corpus ID: 45683839
Reading is a hobby to open the knowledge windows. Besides, it can provide the inspiration and spirit to face this life. By this…
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Highly Cited
1987
Highly Cited
1987
AUTISM AND RETT SYNDROME: BEHAVIOURAL INVESTIGATIONS AND DIFFERENTIAL DIAGNOSIS
B. Rett
Developmental Medicine & Child Neurology
1987
Corpus ID: 23539364
The most common wrong diagnosis of children with Rett syndrome has been the infantile autistic syndrome, and it is probable that…
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Highly Cited
1987
Highly Cited
1987
A quantitative ultrastructural study of rat tendon from birth to maturity.
M. J. Moore
,
Andrew DE Beaux
Journal of Anatomy
1987
Corpus ID: 19786640
In a morphometric analysis of rat tail (RTT) and extensor digitorum longus (EDLT) tendons in rats from birth to 12 weeks of age…
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Highly Cited
1987
Highly Cited
1987
Unilateral brain lesions in childhood: Performance on the revised token test
D. Aram
,
B. Ekelman
Brain and Language
1987
Corpus ID: 36189597
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