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- Challenges in comparing physical abuse, fractures and metabolic bone disease in young children in the UK and SwedenPiers D Mitchell, Richard Brown, Tengyao Wang, Rajen D Shah, Richard J SamworthArchives of Disease in Childhood Jun 2019, archdischild-2019-317457; DOI: 10.1136/archdischild-2019-317457
- Predicting cardiometabolic markers in children using tri-ponderal mass index: a cross-sectional studyJillian Ashley-Martin, Regina Ensenauer, Bryan Maguire, Stefan KuhleArchives of Disease in Childhood Jun 2019, 104 (6) 577-582; DOI: 10.1136/archdischild-2018-316028
- Fifteen years of genetic testing from a London developmental clinicSunayna Best, Elisabeth Rosser, Monika BajajArchives of Disease in Childhood Nov 2017, 102 (11) 1014-1018; DOI: 10.1136/archdischild-2017-312739
- Camp-based family treatment of childhood obesity: randomised controlled trialBeate Benestad, Samira Lekhal, Milada Cvancarova Småstuen, Jens Kristoffer Hertel, Vidar Halsteinli, Rønnaug Astri Ødegård, Jøran HjelmesæthArchives of Disease in Childhood Apr 2017, 102 (4) 303-310; DOI: 10.1136/archdischild-2015-309813
- The prevalence of congenital heart defects in infants with cholestatic disorders of infancy: a single-centre studyAya M Fattouh, Engy A Mogahed, Nehal Abdel Hamid, Rodina Sobhy, Noha Saber, Hanaa El-KaraksyArchives of Disease in Childhood Sep 2016, 101 (9) 803-807; DOI: 10.1136/archdischild-2015-309589
- Recognition, assessment and management of hypoglycaemia in childhoodArunabha Ghosh, Indraneel Banerjee, Andrew A M MorrisArchives of Disease in Childhood Jun 2016, 101 (6) 575-580; DOI: 10.1136/archdischild-2015-308337
- Transformative therapy in hypophosphatasiaNick Bishop, Craig F Munns, Keiichi OzonoArchives of Disease in Childhood Jun 2016, 101 (6) 514-515; DOI: 10.1136/archdischild-2015-309579
- Optimal management of polycystic ovary syndrome in adolescenceNatalie Hecht Baldauff, Silva ArslanianArchives of Disease in Childhood Nov 2015, 100 (11) 1076-1083; DOI: 10.1136/archdischild-2014-306471
- Congenital sucrase–isomaltase deficiency: diagnostic challenges and response to enzyme replacement therapyJ W L Puntis, V ZamvarArchives of Disease in Childhood Sep 2015, 100 (9) 869-871; DOI: 10.1136/archdischild-2015-308388
- Neonatal screening for hereditary tyrosinaemia: are we there yet?Nedim Hadžić, Roshni VaraArchives of Disease in Childhood Aug 2015, 100 (8) 720-721; DOI: 10.1136/archdischild-2015-308265
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