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acquired
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Book Chapter
Published: 17 December 2024
10.1159/000538202
EISBN: 978-3-318-07273-0
...Introduction Acquired platelet disorders occur in childhood. The clinical approach to a child with a suspected acquired platelet disorder includes a careful history, a detailed physical examination, and focused laboratory investigations. Immune thrombocytopenia (ITP) is the most common...
Book Chapter
Published: 17 December 2024
10.1159/000538216
EISBN: 978-3-318-07273-0
...Introduction Acquired bleeding disorders encompass a heterogeneous group of conditions with varied and complex etiology and are typically encountered in hospitalized children with underlying infectious, cardiovascular, neoplastic, hepatic, and renal comorbidities. Diagnosis and management...
Book Chapter
Book: Perspiration Research
Series: Current Problems in Dermatology
Volume: 51
Published: 01 September 2016
10.1159/000446781
EISBN: 978-3-318-05905-2
... Abstract Acquired idiopathic generalized anhidrosis (AIGA) is a sweating disorder characterized by inadequate sweating in response to heat stimuli such as high temperature, humidity, and physical exercise. Patients exhibit widespread nonsegmental hypohidrosis/anhidrosis without any apparent...
Book Chapter
Series: Advances in Oto-Rhino-Laryngology
Volume: 79
Published: 03 August 2016
10.1159/000445134
EISBN: 978-3-318-05854-3
... in the maintenance of normal epithelial function has revealed that mild and variable CFTR mutations play a causative role in a number of diseases not classically associated with CF. Furthermore, recent evidence indicates that acquired defects in wild-type CFTR protein processing, endocytic recycling and function can...
Book Chapter
Published: 20 June 2013
10.1159/000346955
EISBN: 978-3-318-02198-1
.... Semin Dial 2009;22:279-286 24. Hedges SJ, et al: Evidence-based treatment recommendations for uremic bleeding. Nat Clin Pract Nephrol 2007;3:138-153 25. Collins PW, et al: Acquired hemophilia A in the United Kingdom: a 2-year national surveillance study by the United Kingdom Haemophilia Centre...
Book Chapter
Series: Endocrine Development
Volume: 19
Published: 17 June 2010
10.1159/000316893
EISBN: 978-3-8055-9451-6
... or the adipose transcription factor PPARΓ. Importantly, lamin A/Cmutations are also responsible for metabolic laminopathies, resembling the metabolic syndrome and progeria, a syndrome of premature aging. A number of lipodystrophic patients remain undiagnosed at the genetic level. Acquired lipodystrophy can...
Book Chapter
Book: Paediatric Bronchoscopy
Series: Progress in Respiratory Research
Volume: 38
Published: 06 May 2010
10.1159/000314390
EISBN: 978-3-8055-9311-3
... and the indications for endoscopy with regard to the upper airways. The main focus is on the aetiology, frequency, endoscopic appearance and typical clinical presentation of important congenital and acquired abnormalities of the nose, pharynx and larynx. The nasopharyngeal lesions discussed include choanal stenosis...
Book Chapter
Book: Paediatric Bronchoscopy
Series: Progress in Respiratory Research
Volume: 38
Published: 06 May 2010
10.1159/000314391
EISBN: 978-3-8055-9311-3
... studies exist that clearly describe how to interpret and classify structural abnormalities of the bronchial tree and quantify their contribution to clinical respiratory pathology. In this chapter, we try to describe the main congenital and acquired abnormalities of the lower airways as they appear...
Book Chapter
Published: 15 October 2008
10.1159/000177241
EISBN: 978-3-8055-8660-3
... Abstract Acquired hemophilia A is a rare immune coagulopathy causing life- or limb-threatening bleeding episodes.Responsible autoantibody inhibitors against factor VIII coagulant protein appear spontaneouslyin subjects with previously normal hemostatic function. Despite the fact that hemostatic...
Book Chapter
Published: 15 October 2008
10.1159/000177251
EISBN: 978-3-8055-8660-3
... diathesis. Consequently,in contrast to inherited platelet disorders, acquired platelet function defects are much more frequentin clinical practice and therefore deserve special attention. Their pathogenesis is widespread and heterogeneouswith various, sometimes overlapping abnormalities in the same clinical...
Book Chapter
Series: Progress in Respiratory Research
Volume: 36
Published: 29 May 2007
10.1159/000102698
EISBN: 978-3-318-01377-1
... Abstract Pulmonary alveolar proteinosis (PAP) is a rare disordercharacterized by abundant deposition of surfactant-like materialin the aveoli. In this article we focus the discussion on theprimary acquired (idiopathic) PAP. We report the studies thatdeveloped the concept that this disorder...
Book Chapter
Published: 27 April 2007
10.1159/000101822
EISBN: 978-3-318-01447-1
Book Chapter
Series: Current Directions in Autoimmunity
Volume: 9
Published: 19 December 2005
10.1159/000090769
EISBN: 978-3-318-01294-1
Book Chapter
Series: Monographs in Oral Science
Volume: 19
Published: 02 December 2005
10.1159/000090585
EISBN: 978-3-318-01247-7
Book Chapter
Book: Uveitis Update
Series: Developments in Ophthalmology
Volume: 31
Published: 20 September 1999
10.1159/000060766
EISBN: 978-3-318-00445-8
Book Chapter
Series: Contributions to Oncology
Volume: 42
Published: 06 November 1992
10.1159/000421308
EISBN: 978-3-318-03425-7
Book
Book Chapter
Series: Contributions to Nephrology
Volume: 100
Published: 30 September 1992
10.1159/000421463
EISBN: 978-3-318-03364-9
Book Chapter
Series: Antibiotics and Chemotherapy
Volume: 43
Published: 14 May 1991
10.1159/000419733
EISBN: 978-3-318-03218-5
Book Chapter
Series: Contributions to Nephrology
Volume: 88
Published: 08 February 1991
10.1159/000419538
EISBN: 978-3-318-03352-6
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