The use of AlloDerm in postmastectomy alloplastic breast reconstruction: part II. A cost analysis
LA Jansen, SA Macadam - Plastic and reconstructive surgery, 2011 - journals.lww.com
Background: Increasingly, AlloDerm is being used in alloplastic breast reconstruction, and
has been the subject of a recent systematic review. The authors' objective was to perform a …
has been the subject of a recent systematic review. The authors' objective was to perform a …
The use of AlloDerm in postmastectomy alloplastic breast reconstruction: part I. A systematic review
LA Jansen, SA Macadam - Plastic and reconstructive surgery, 2011 - journals.lww.com
Background: Postmastectomy alloplastic breast reconstruction is a common procedure that
continues to evolve. Increasingly, AlloDerm is being used in both direct-to-implant and two …
continues to evolve. Increasingly, AlloDerm is being used in both direct-to-implant and two …
The evidence base for the acellular dermal matrix AlloDerm: a systematic review
LA Jansen, P De Caigny, NA Guay… - Annals of plastic …, 2013 - journals.lww.com
Background Many decellularized dermal matrices are available with various applications, all
with slight differences. AlloDerm appears to have the greatest presence in the literature. The …
with slight differences. AlloDerm appears to have the greatest presence in the literature. The …
PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasia
Malformations of cortical development containing dysplastic neuronal and glial elements,
including hemimegalencephaly and focal cortical dysplasia, are common causes of …
including hemimegalencephaly and focal cortical dysplasia, are common causes of …
Association of MTOR mutations with developmental brain disorders, including megalencephaly, focal cortical dysplasia, and pigmentary mosaicism
GM Mirzaa, CD Campbell, N Solovieff, CP Goold… - JAMA …, 2016 - jamanetwork.com
Importance Focal cortical dysplasia (FCD), hemimegalencephaly, and megalencephaly
constitute a spectrum of malformations of cortical development with shared neuropathologic …
constitute a spectrum of malformations of cortical development with shared neuropathologic …
Impaired glial glutamate transport in a mouse tuberous sclerosis epilepsy model
Excessive astrocytosis in cortical tubers in tuberous sclerosis complex (TSC) suggests that
astrocytes may be important for epileptogenesis in TSC. We previously demonstrated that …
astrocytes may be important for epileptogenesis in TSC. We previously demonstrated that …
Novel mutations in ATP1A3 associated with catastrophic early life epilepsy, episodic prolonged apnea, and postnatal microcephaly
AR Paciorkowski, SS McDaniel, LA Jansen, H Tully… - …, 2015 - Wiley Online Library
Summary Objective Mutations of ATP 1A3 have been associated with rapid onset dystonia‐
parkinsonism and more recently with alternating hemiplegia of childhood. Here we report …
parkinsonism and more recently with alternating hemiplegia of childhood. Here we report …
[HTML][HTML] Unrealistic optimism in early-phase oncology trials
Early-phase oncology trials are vital for developing new and more effective therapies for
treating cancers. While it is possible that some of these trials provide benefit to …
treating cancers. While it is possible that some of these trials provide benefit to …
[HTML][HTML] Untargeted metabolomics and infrared ion spectroscopy identify biomarkers for pyridoxine-dependent epilepsy
UFH Engelke, RE Van Outersterp… - The Journal of …, 2021 - Am Soc Clin Investig
Background Pyridoxine-dependent epilepsy (PDE-ALDH7A1) is an inborn error of lysine
catabolism that presents with refractory epilepsy in newborns. Biallelic ALDH7A1 variants …
catabolism that presents with refractory epilepsy in newborns. Biallelic ALDH7A1 variants …
Abnormal glutamate homeostasis and impaired synaptic plasticity and learning in a mouse model of tuberous sclerosis complex
LH Zeng, Y Ouyang, V Gazit, JR Cirrito, LA Jansen… - Neurobiology of …, 2007 - Elsevier
Mice with inactivation of the Tuberous sclerosis complex-1 (Tsc1) gene in glia
(Tsc1GFAPCKO mice) have deficient astrocyte glutamate transporters and develop seizures …
(Tsc1GFAPCKO mice) have deficient astrocyte glutamate transporters and develop seizures …