Search Results - "Lau, Gene T. C."

EWSR1-CREB3L1 gene fusion: a novel alternative molecular aberration of low-grade fibromyxoid sarcoma by Lau, Patrick P L, Lui, Philip C W, Lau, Gene T C, Yau, Derek T W, Cheung, Elaine T Y, Chan, John K C

“…Low-grade fibromyxoid sarcoma (LGFMS) is an uncommon sarcoma with a deceptively bland-looking morphology that disguises its malignant clinical behavior. It…”
Get full text

Adenofibromatous Solitary Fibrous Tumor: An Unusual Morphologic Variant Occurring in the Sinonasal Tract by Kwok, Angie L. M., Chan, John K. C., Tang, Alexander H. N., Luk, Ivy S. C., Lau, Gene T. C., Cheuk, Wah

“…Background Solitary fibrous tumor can exhibit a broad morphologic spectrum, such as presence of epithelioid tumor cells, adipose cells and multinucleated giant…”
Get full text

Metallic implant-associated lymphoma : A distinct subgroup of large b-cell lymphoma related to pyothorax-associated lymphoma? by CHEUK, Wah, CHAN, Alexander C. L, CHAN, John K. C, LAU, Gene T. C, CHAN, Vincent N. H, YIU, Harry H. Y

“…Primary non-Hodgkin lymphoma arising at the site of metallic implant is very rare, and the possible carcinogenic effects of the metallic components and wear…”
Get full text

Is gliomatosis peritonei derived from the associated ovarian teratoma? by Kwan, Man-Yee, Kalle, Wouter, Lau, Gene T.C, Chan, John K.C

“…Gliomatosis peritonei, a rare condition that occurs almost exclusively in the setting of ovarian immature teratoma, is characterized by the occurrence of…”
Get full text

Hyperammonaemic encephalopathy in an adult patient with citrin deficiency associated with a novel mutation by Ng, Y W, Chan, Angel O K, Au Yeung, Y T, Lau, Gene T C, Cheng, C W, Shek, C C, Tiu, S C

“…We report on an adult patient with citrin deficiency in Hong Kong, in whom a novel mutation was identified. The patient presented with recurrent…”
Get full text

A rare cause of nephrotic syndrome: lipoprotein glomerulopathy by Cheung, C Y, Chan, Angel O K, Chan, Y H, Lee, K C, Chan, Gordon P T, Lau, Gene T C, Shek, C C, Chau, K F, Li, C S

“…Lipoprotein glomerulopathy is a rare kidney disease in which lipoprotein thrombi are seen in the glomerular capillaries. Most of these patients are found in…”
Get full text

Diagnosis of 5alpha-reductase 2 deficiency: a local experience by Chan, Angel O K, But, Betty W M, Lau, Gene T C, Lam, Almen L N, Ng, K L, Lam, Y Y, Lee, C Y, Shek, C C

“…5Alpha-reductase 2 deficiency is an autosomal recessive disorder characterised by lack of masculinisation in XY individuals due to failure to convert…”
Get full text

Enzyme replacement therapy for infantile Pompe disease during the critical period and identification of a novel mutation by But, W M, Lee, S H, Chan, Angel O K, Lau, Gene T C

“…Pompe disease (acid maltase deficiency, glycogen storage disease type II) is a rare progressive autosomal recessive disorder caused by a deficiency of…”
Get full text

Hepatitis B virus DNA in peripheral blood leukocytes. A comparison between hepatocellular carcinoma and other hepatitis B virus-related chronic liver diseases by Leung, N W, Tam, J S, Lau, G T, Leung, T W, Lau, W Y, Li, A K

“…Hepatitis B virus (HBV) DNA has been detected in the peripheral blood leukocytes (PBL) during acute and chronic HBV infection. Possible pathobiologic…”
Get more information

Bacteriologic analyses of bile and brown pigment stones in patients with acute cholangitis by Leung, Joseph W., Liu, Yan-lei, Lau, Gene C.T., Chan, Raphael C.Y., Lai, Alex C.W., Ling, Thomas K.W., Cheng, Augustine F.

“…Background: Bacteria play an important role in the formation of brown pigment stones through adherence and biofilm formation. Scanning electron microscopy of…”
Get full text