List of works - Ming-Jen Lee

A case of familial amyloidotic polyneuropathy with a rare Phe33Leu mutation in the TTR gene

scientific article published on 15 September 2012

A novel SCN9A mutation responsible for primary erythromelalgia and is resistant to the treatment of sodium channel blockers

scientific article

A novel XK gene mutation in a Taiwanese family with McLeod syndrome.

scientific article published on 27 February 2014

Acute intermittent porphyria with peripheral neuropathy: a follow-up study after hematin treatment

scientific article published on 24 April 2007

Arg332Cys mutation of NOTCH3 gene in the first known Taiwanese family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

scientific article published on 24 December 2004

BST1 rs11724635 interacts with environmental factors to increase the risk of Parkinson's disease in a Taiwanese population.

scientific article published on 20 November 2013

Cerebral amyloid angiopathy in East and West.

scientific article published on October 2010

Characterization of a familial case with primary erythromelalgia from Taiwan.

scientific article

Clinical presentations and skin denervation in amyloid neuropathy due to transthyretin Ala97Ser.

scientific article published on August 2010

Comparison of two PCR-based molecular methods in the diagnosis of CMT 1A and HNPP diseases in Chinese.

scientific article

Complex haplotypic effects of the ABCB1 gene on epilepsy treatment response.

scientific article published in June 2005

Cutaneous and sympathetic denervation in neonatal rats with a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 gene.

scientific article

Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutation.

scientific article published on 3 March 2009

Genotype-phenotype correlates in Taiwanese patients with early-onset recessive Parkinsonism.

scientific article

HMBS mutations in Chinese patients with acute intermittent porphyria.

scientific article published in September 2008

Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4 ) gene

scientific journal article

Leptin induces migration and invasion of glioma cells through MMP-13 production.

scientific article published on March 2009

Longitudinal evaluation of an N-ethyl-N-nitrosourea-created murine model with normal pressure hydrocephalus

scientific article (publication date: 2009)

Mutations of the SPG11 gene in patients with autosomal recessive spastic paraparesis and thin corpus callosum

scientific article published on 01 May 2008

Neurological complications of acute intermittent porphyria

scientific article published on 4 October 2011

Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke.

scientific article published on 18 January 2006

Overweight modulates APOE and APOA5 alleles on the risk of severe hypertriglyceridemia.

scientific article published on 23 November 2012

Purple pigments: the pathophysiology of acute porphyric neuropathy.

scientific article published on 19 August 2011

Six novel NPC1 mutations in Chinese patients with Niemann-Pick disease type C.

scientific article

Six novel connexin32 (GJB1) mutations in X-linked Charcot-Marie-Tooth disease.

scientific article

The Influences of Reserpine and Imipramine on the 5-HT2 Receptor Binding Site and Its Coupled Second Messenger in Rat Cerebral Cortex

scientific article published on August 31, 2013

The MicroRNA Spectrum in 12 Body Fluids ⬇️

scientific article (publication date: November 2010)

The systems biology of neurofibromatosis type 1--critical roles for microRNA.

scientific article published on 31 October 2011

Valosin-containing protein and neurofibromin interact to regulate dendritic spine density ⬇️

scientific article published on November 21, 2011

rs5848 variant of progranulin gene is a risk of Alzheimer's disease in the Taiwanese population.

scientific article published on 7 January 2011

List of works by Ming-Jen Lee

A case of familial amyloidotic polyneuropathy with a rare Phe33Leu mutation in the TTR gene

A novel SCN9A mutation responsible for primary erythromelalgia and is resistant to the treatment of sodium channel blockers

A novel XK gene mutation in a Taiwanese family with McLeod syndrome.

Acute intermittent porphyria with peripheral neuropathy: a follow-up study after hematin treatment

Arg332Cys mutation of NOTCH3 gene in the first known Taiwanese family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

BST1 rs11724635 interacts with environmental factors to increase the risk of Parkinson's disease in a Taiwanese population.

Cerebral amyloid angiopathy in East and West.

Characterization of a familial case with primary erythromelalgia from Taiwan.

Clinical presentations and skin denervation in amyloid neuropathy due to transthyretin Ala97Ser.

Comparison of two PCR-based molecular methods in the diagnosis of CMT 1A and HNPP diseases in Chinese.

Complex haplotypic effects of the ABCB1 gene on epilepsy treatment response.

Cutaneous and sympathetic denervation in neonatal rats with a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 gene.

Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutation.

Genotype-phenotype correlates in Taiwanese patients with early-onset recessive Parkinsonism.

HMBS mutations in Chinese patients with acute intermittent porphyria.

Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4 ) gene

Leptin induces migration and invasion of glioma cells through MMP-13 production.

Longitudinal evaluation of an N-ethyl-N-nitrosourea-created murine model with normal pressure hydrocephalus

Mutations of the SPG11 gene in patients with autosomal recessive spastic paraparesis and thin corpus callosum

Neurological complications of acute intermittent porphyria

Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke.

Overweight modulates APOE and APOA5 alleles on the risk of severe hypertriglyceridemia.

Purple pigments: the pathophysiology of acute porphyric neuropathy.

Six novel NPC1 mutations in Chinese patients with Niemann-Pick disease type C.

Six novel connexin32 (GJB1) mutations in X-linked Charcot-Marie-Tooth disease.

The Influences of Reserpine and Imipramine on the 5-HT2 Receptor Binding Site and Its Coupled Second Messenger in Rat Cerebral Cortex

The MicroRNA Spectrum in 12 Body Fluids ⬇️

The systems biology of neurofibromatosis type 1--critical roles for microRNA.

Valosin-containing protein and neurofibromin interact to regulate dendritic spine density ⬇️

rs5848 variant of progranulin gene is a risk of Alzheimer's disease in the Taiwanese population.