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   Table of Contents
Coverpage
September-December 2012
Volume 5 | Issue 3
Page Nos. 191-378

Online since Tuesday, April 24, 2018

Accessed 243 times.

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EDITORIAL  

Newborn screening in the Middle East and North Africa – challenges and recommendations p. 191
Rabah M Shawky
DOI:10.7707/hmj.v5i3.192  
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HISTORICAL REVIEW Top

The lifework of Erich Saling – the father of perinatal medicine p. 193
Monika Drager, Asim Kurjak
DOI:10.7707/hmj.v5i3.179  
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STATE-OF-THE-ART REVIEW Top

The very low-birthweight infant p. 199
Arnold Pollak, Rachel Weitzdoerfer
DOI:10.7707/hmj.v5i3.198  
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Prenatal diagnosis p. 213
Erich Hafner
DOI:10.7707/hmj.v5i3.196  
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Surgical treatment of neonatal intestinal malformations p. 223
Rebecca Jasmine Hahn
DOI:10.7707/hmj.v5i3.202  
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REVIEW FOR THE SHEIKH HAMDAN BIN RASHID AL MAKTOUM AWARD FOR MEDICAL SCIENCES Top

Comments on the past and predictions on the future of neonatal research – consortia, randomized cluster trials, brain care centres and xenon p. 245
Jerold F Lucey
DOI:10.7707/hmj.v5i3.183  
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Are we improving long-term outcomes for extremely preterm babies? p. 249
Lex W Doyle
DOI:10.7707/hmj.v5i3.185  
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Community-based strategies for newborn care: evidence for scaling up in developing countries p. 257
Zulfiqar Bhutta
DOI:10.7707/hmj.v5i3.194  
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The molecular basis of pulmonary surfactant – lessons from newborn infants p. 263
Jeffrey A Whitsett
DOI:10.7707/hmj.v5i3.180  
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Epigenetics and nutrition – nature versus nurture p. 273
Rebecca Simmons
DOI:10.7707/hmj.v5i3.210  
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The causation of neural tube defects – a journey of discovery and the challenge of prevention p. 285
Nicholas J Wald
DOI:10.7707/hmj.v5i3.211  
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The exploitation of extracellular nucleic acids in diagnosis and prediction of placental insufficiency-related complications p. 293
Ilona Hromadnikova
DOI:10.7707/hmj.v5i3.182  
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Infant and fetal vitamin D status and bone health p. 297
John M Pettifor
DOI:10.7707/hmj.v5i3.186  
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Al-Aqeel Sewairi syndrome, MIM#605156, a prototype for personalized medicine for the study and prevention of genetic metabolic disorders in Saudi Arabia p. 305
Aida I Al-Aqeel
DOI:10.7707/hmj.v5i3.187  
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Clinical, biochemical and genetic aspects of peroxisomal disorders – an expanding group of genetic diseases in humans p. 313
Ronald J A Wanders
DOI:10.7707/hmj.v5i3.212  
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Pathway-restoring therapies – an update on serine and on mannose treatment p. 327
Jaak Jaeken
DOI:10.7707/hmj.v5i3.188  
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In utero haematopoietic stem cell transplantation – experimental progress towards clinical application p. 333
Alan W Flake
DOI:10.7707/hmj.v5i3.189  
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Caffeine therapy for apnoea of prematurity in very low-birthweight infants p. 345
Barbara Schmidt, Arne Ohlsson, Peter G Davis
DOI:10.7707/hmj.v5i3.190  
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Classical homocystinuria: newborn screening with early treatment effectively prevents complications p. 351
Sufin Yap
DOI:10.7707/hmj.v5i3.191  
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Biochemical profiling of inborn errors of purine and pyrimidine metabolism by high-performance liquid chromatography – a strategy to improve childhood mortality and morbidity in Malaysian children p. 363
Bee Chin Chen, Meow Keong Thong, Zabedah M Yunus
DOI:10.7707/hmj.v5i3.174  
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COMMENTS: PAEDIATRICS AND GENETICS Top

Sudden unexplained death in the young – a genetic approach to non-structural cardiac defects p. 373
Rabah M Shawky
DOI:10.7707/hmj.v5i3.134  
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CASE REPORT Top

Antenatal diagnosis of ectrodactyly with fibular aplasia – a case report p. 375
Nawal M Hubaishi, Fatima Cherifi
DOI:10.7707/hmj.v5i3.151  
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