Results 141 to 150 of about 20,847 (184)

Treatment for Hyperosmolar Dehydration in Hospitalised Adults: Protocol for a Scoping Review of Current Evidence and Gaps. [PDF]

JMIR Res Protoc
Hansen CH, Mortensen LT, Brandstrup B, Beck AM, Andersen S, Danielsen MB.   +5 more
europepmc   +1 more source

Complication rates of 16- and 18-gauge needles for native kidney biopsies: a systematic review and proportional meta-analysis. [PDF]

Ren Fail
Møller M, Andersen TH, Borg R, Christensen R, Bressendorff I, Hansen EK, Rønnemoes R, Jakobsen SK, Haar K, Persson F, Rossing P, Hansen D.   +11 more
europepmc   +1 more source

Genetic biomarkers associated with risk and therapeutic response in erectile dysfunction: a systematic review. [PDF]

Front Pharmacol
Ferezin LP, Kayzuka C, Paiva de Alcântara E Silva M, Tavares Peixeiro CN, Rondon-Pereira VC, Tanus-Santos JE, Lacchini R.   +6 more
europepmc   +1 more source

Early-Onset Neonatal Infection and Cerebral Palsy.

JAMA Netw Open
Andersen M, Matthiesen NB, Murra M, Nielsen SY, Henriksen TB.   +4 more
europepmc   +1 more source

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Andersen-Tawil syndrome

International Journal of Cardiology, 2011
Advances in the understanding of genetic aspects of cardiovascular diseases, together with an increase in the availability of genetic analysis, have resulted in not only increased diagnosis of known inherited conditions, but also the identification of novel syndromes.
Robin Weir, Victoria Murday
exaly   +2 more sources

Andersen syndrome autosomal dominant in three generations

American Journal of Medical Genetics, 1999
Andersen syndrome is a rare entity and comprises potassium sensitive periodic paralysis, ventricular arrhythmia, and an unusual facial appearance; syncope and sudden death have also been reported. The recognition of the characteristic face permits an early diagnosis in order to detect the severe systemic manifestations that are associated with this ...
S, Canún, N, Pérez, L G, Beirana
exaly   +3 more sources

Andersen–Tawil syndrome: Clinical and molecular aspects

International Journal of Cardiology, 2013
Andersen–Tawil syndrome (ATS) is a rare hereditary multisystem disorder. Ventricular arrhythmias, periodic paralysis and dysmorphic features constitute the classic triad of ATS symptoms. The expressivity of these symptoms is, however, extremely variable, even within single ATS affected families, and not all ATS patients present with the full triad of ...
Ronald Wilders
exaly   +3 more sources

Andersen-Tawil syndrome

Andersen-Tawil syndrome (ATS) is one of the periodic paralyses, a set of skeletal muscle disorders that cause transient weakness of the arms and legs lasting minutes to many hours. Distinguishing features of ATS include facial and limb dysmorphisms, cardiac arrhythmia, difficulties with executive function, and association with dominant mutations in the
Jill A, Goslinga, Louis J, PtáČek, Rabi, Tawil, Alexander, Fay   +3 more
openaire   +2 more sources

Cardiac Surgery for a Patient With Andersen-Tawil Syndrome

The Annals of Thoracic Surgery, 2010
Andersen-Tawil syndrome is an uncommon inherited autosomal disorder characterized by a prolonged QT interval, periodic paralysis, and dysmorphic features. The deleterious effects of cardioplegia on periodic paralysis and cardiac arrhythmia are unknown, and no studies have reported the performance of cardiac surgery in patients with Andersen-Tawil ...
Mitsugi, Nagashima, Takashi, Higaki, Yoshimasa, Seike, Yuichiro, Yokoyama   +3 more
openaire   +2 more sources

Andersen-Tawil and Timothy Syndromes

2013
This chapter summarizes two relatively new ion channelopathies, Andersen-Tawil and Timothy syndromes. Both disorders are pleiotropic in nature, with multiple clinical manifestations outside the cardiovascular system. While both Andersen-Tawil and Timothy syndromes are disorders of ventricular repolarization, their unique clinical phenotype ...
Martin Tristani-Firouzi, Susan P. Etheridge   +1 more
openaire   +1 more source