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The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|April 30, 2008
Outcome of heart transplants 15 to 20 years ago: graft survival, post-transplant morbidity, and risk factors for mortalityJean C Roussel, Olivier Baron, Christian Périgaud, et al.
Pediatrics|October 1, 1996
Idiopathic disseminated bacillus Calmette-Guérin infection: a French national retrospective studyJ L Casanova, S Blanche, J F Emile, et al.
Nature Communications|November 10, 2016
Decrease of SYNGAP1 in GABAergic cells impairs inhibitory synapse connectivity, synaptic inhibition and cognitive functionMartin H Berryer, Bidisha Chattopadhyaya, Paul Xing, et al.
Contemporary Clinical Trials|November 5, 2019
Preventing diabetes with digital health and coaching for translation and scalability (PREDICTS): A type 1 hybrid effectiveness-implementation trial protocolFabio A Almeida, Tzeyu L Michaud, Kathryn E Wilson, et al.
American Journal of Human Genetics|October 1, 2013
Recessive and dominant mutations in retinoic acid receptor beta in cases with microphthalmia and diaphragmatic herniaMyriam Srour, David Chitayat, Véronique Caron, et al.
Plos Genetics|September 24, 2010
Mice doubly-deficient in lysosomal hexosaminidase A and neuraminidase 4 show epileptic crises and rapid neuronal lossVolkan Seyrantepe, Pablo Lema, Aurore Caqueret, et al.
Clinical Genetics|September 9, 2016
Loss of the proprioception and touch sensation channel PIEZO2 in siblings with a progressive form of contracturesA A Mahmud, N A Nahid, C Nassif, et al.
Biological Psychiatry|January 18, 2011
De novo SYNGAP1 mutations in nonsyndromic intellectual disability and autismFadi F Hamdan, Hussein Daoud, Amélie Piton, et al.
BMC Medical Genomics|March 29, 2011
Comparison of genome-wide array genomic hybridization platforms for the detection of copy number variants in idiopathic mental retardationTracy Tucker, Alexandre Montpetit, David Chai, et al.
HGG Advances|November 5, 2025
CUL1 variants cause severe neurodevelopmental disorders: Insights from human genetics and a zebrafish model of microcephalyHaoling Xu, Zhen Liu, Fadi F Hamdan, et al.
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