STUVE-WIEDEMANN SYNDROME

Known as: SCHWARTZ-JAMPEL SYNDROME, NEONATAL, STUVE-WIEDEMANN/SCHWARTZ-JAMPEL TYPE 2 SYNDROME, Stuve-Wiedemann-Schwartz-Jampel type 2 syndrome 
 
National Institutes of Health

Papers overview

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2014
2014
Stuve-Wiedemann Syndrome (SWS) (OMIM #601559) is an autosomal recessive disorder characterized by skeletal changes, bowing of the… (More)
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2014
2014
A woman was isozygous for a novel mutation in the leukemia inhibitory factor receptor gene (LIFR) (c.2170C>G; p.Pro724Ala) which… (More)
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2010
2010
Stüve-Wiedemann syndrome (SWS, OMIM 601559) is a severe autosomal recessive condition caused by mutations in the leukemia… (More)
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Review
2010
Review
2010
Functional brain imaging has been used in humans to noninvasively investigate the neural mechanisms underlying the generation of… (More)
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Highly Cited
2010
Highly Cited
2010
OBJECTIVE To investigate whether age-related and experimental reductions in SWS and sleep continuity are associated with… (More)
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Highly Cited
2005
Highly Cited
2005
Spectral estimates of heart rate variability (HRV) often involve the use of techniques such as the fast Fourier transform (FFT… (More)
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2005
2005
OBJECTIVES To evaluate the additional information provided by pulse transit time (PTT), a noninvasive tool, when using during… (More)
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2003
2003
In this study a number of analytical procedures are described to determine pharmaceuticals and personal care products (PPCPs) and… (More)
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Review
2002
Review
2002
The human sleep-wake cycle is generated by a circadian process, originating from the suprachiasmatic nuclei, in interaction with… (More)
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Highly Cited
1996
Highly Cited
1996
During recent years, methods from nonlinear dynamics were introduced into the analysis of EEG signals. Although from a… (More)
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