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Showing 101-120 of 435 results
  1. SPR 2020

    Article 20 May 2020
  2. The complete European guidelines on phenylketonuria: diagnosis and treatment

    Abstract

    Phenylketonuria (PKU) is an autosomal recessive inborn error of phenylalanine metabolism caused by deficiency in the enzyme phenylalanine...

    A. M. J. van Wegberg, A. MacDonald, ... F. J. van Spronsen in Orphanet Journal of Rare Diseases
    Article Open access 12 October 2017
  3. Severe congenital neutropenias

    Severe congenital neutropenias are a heterogeneous group of rare haematological diseases characterized by impaired maturation of neutrophil...

    Julia Skokowa, David C. Dale, ... Karl Welte in Nature Reviews Disease Primers
    Article 08 June 2017
  4. Complementary traditional Chinese medicine use in Children with cerebral palsy: a nationwide retrospective cohort study in Taiwan

    Background

    Complementary traditional Chinese medicine (TCM) has been used to treat patients with cerebral palsy (CP). However, large-scale surveys...

    Hou-Hsun Liao, Hung-Rong Yen, ... Tung-Ti Chang in BMC Complementary and Alternative Medicine
    Article Open access 14 March 2017
  5. The etiology and significance of fractures in infants and young children: a critical multidisciplinary review

    This paper addresses significant misconceptions regarding the etiology of fractures in infants and young children in cases of suspected child abuse....

    Sabah Servaes, Stephen D. Brown, ... Thomas L. Slovis in Pediatric Radiology
    Article 17 February 2016
  6. Contraceptive Considerations for Women with Gastrointestinal Disorders

    Gastroenterologists are in a unique position to assist women with chronic gastrointestinal disorders in order to optimize their health prior to...

    Aparna Sridhar, Carrie A. Cwiak, ... Rebecca H. Allen in Digestive Diseases and Sciences
    Article 24 November 2016
  7. Adjuvant ovarian suppression for resected breast cancer: 2017 critical assessment

    Currently available data supporting adjuvant ovarian function suppression for resected breast cancer in premenopausal women in addition to standard...

    Article 10 July 2017
  8. Primary immunodeficiency associated with chromosomal aberration – an ESID survey

    Background

    Patients with syndromic features frequently suffer from recurrent respiratory infections, but little is known about the spectrum of...

    Ellen Schatorjé, Michiel van der Flier, ... Esther de Vries in Orphanet Journal of Rare Diseases
    Article Open access 02 August 2016
  9. Osteogenesis imperfecta–A tale of 50 years

    Preeti Singh, Anju Seth in Indian Pediatrics
    Article 24 December 2015
  10. Outcome of esophageal atresia/tracheoesophageal fistula in extremely low birth weight neonates (<1000 grams)

    Purpose

    To review the outcomes of extremely low birth weight (ELBW, <1000 g) infants with esophageal atresia/tracheoesophageal fistula (EA/TEF).

    ...
    Augusto Zani, Justyna Wolinska, ... Agostino Pierro in Pediatric Surgery International
    Article 30 October 2015
  11. Minerals and extremely low birth weight infants

    Guglielmo Salvatori, Silvia Foligno in Italian Journal of Pediatrics
    Article Open access 24 September 2015
  12. Bone status in preterm infant: influences of different nutritional regimens and possible markers of bone disease

    Objective:

    The objective of this study was to evaluate possible influences of parenteral nutrition on growth and bone development in preterms and to...

    M Meneghelli, A Pasinato, ... G Verlato in Journal of Perinatology
    Article 14 January 2016
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