✦ LIBER ✦

Chiari type I malformation in children and adolescents with cystic fibrosis

✍ Scribed by Joshua P. Needleman; Howard B. Panitch; Karin S. Bierbrauer; Daniel V. Schidlow

Publisher: John Wiley and Sons
Year: 2000
Tongue: English
Weight: 19 KB
Volume: 30
Category: Article
ISSN: 8755-6863
DOI: 10.1002/1099-0496(200012)30:6<490::aid-ppul9>3.0.co;2-i

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Lower respiratory illness in infants and

Lower respiratory illness in infants and young children with cystic fibrosis

✍ Robert S. Tepper; H. Eigen; J. Stevens; C. Angelicchio; J. Kisling; W. Ambrosius 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 30 KB 👁 2 views

The purpose of our study was to assess the effect on pulmonary function of adding intravenous hydrocortisone to the standard treatment of infants with cystic fibrosis (CF) hospitalized for lower respiratory illnesses (LRI). Twenty CF infants were randomized and received 10 days of hydrocortisone (10

Adult Arnold-Chiari malformation type I

Adult Arnold-Chiari malformation type I associated with an aseptic meningeal reaction

✍ M. Seth Hochman; Steven A. Kobetz 📂 Article 📅 1981 🏛 John Wiley and Sons 🌐 English ⚖ 217 KB

Sun and Streib [3] , in their review of the literature on diabetic thoracoabdominal neuropathy, accidentally omitted a large series of this entity. Ellenberg Ill reported 40 patients with "diabetic truncal mononeuropathy" in 1978. Characteristics of his cases differed in some aspects from the 5 pat

Management of chronic sinusitis in child

Management of chronic sinusitis in children with cystic fibrosis

✍ Max M. April 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 182 KB 👁 2 views

Sweat electrolyte and cystic fibrosis mu

Sweat electrolyte and cystic fibrosis mutation analysis allows early diagnosis in Brazilian children with clinical signs compatible with cystic fibrosis

✍ Rabbi-Bortolini, Eliete; Bernardino, Andr�a L.F.; Lopes, Adoris L.; Ferri, Adria 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 24 KB 👁 2 views

A total of 540 individuals with clinical signs suggestive of cystic fibrosis (CF) was studied. The sweat chloride was measured and the DF508, G542X, R553X, and W1282X mutations of the CF gene were screened by polymerase chain reaction (PCR). With this approach the diagnosis of CF was confirmed in 12

Size of pancreas in children and adolesc

Size of pancreas in children and adolescents with type I (insulin-dependent) diabetes

✍ Altobelli, Emma; Blasetti, Annalisa; Verrotti, Alberto; Di Giandomenico, Vincenz 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 152 KB 👁 2 views

Purpose. The aim of this study was to evaluate the influence of insulin-dependent diabetes mellitus (IDDM) on the size of the pancreas in children. Methods. Pancreas size was evaluated sonographically in a group of 60 diabetic children and adolescents, aged 3-15 years, and 60 sex-and age-matched he

Diagnostic accuracy of oropharyngeal cul

Diagnostic accuracy of oropharyngeal cultures in infants and young children with cystic fibrosis

✍ Margaret Rosenfeld; Julia Emerson; Frank Accurso; David Armstrong; Robert Castil 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 77 KB 👁 2 views

The objective of this study was to assess the diagnostic accuracy of oropharyngeal (OP) cultures relative to simultaneous bronchoalveolar lavage (BAL) cultures in very young children with CF, and to examine the effects of bacterial density, age, and study cohort on diagnostic accuracy. Respiratory c