Event Videos

http://www.ncbi.nlm.nih.gov/pubmed/25716872

Gonzales E, Grosse B, Schuller B, Davit-Spraul A, Conti F, Guettier C, Cassio D, Jacquemin E. Targeted pharmacotherapy in progressive familial intrahepatic cholestasis type 2: Evidence for improvement of cholestasis with 4-phenylbutyrate. Hepatology. 2015 Aug; 62(2):558-66.

Abstract

Published on: 
Aug-2015

http://www.ncbi.nlm.nih.gov/pubmed/25851052

- hepatitis b

Chen HL, Lee CN, Chang CH, Ni YH, Shyu MK, Chen SM, Hu JJ, Lin HH, Zhao LL, Mu SC, Lai MW, Lee CL, Lin HM, Tsai MS, Hsu JJ, Chen DS, Chan KA, Chang MH; Taiwan Study Group for the Prevention of Mother-to-Infant Transmission of HBV (PreMIT Study); Taiwan Study Group for the Prevention of Mother-to-Infant Transmission of HBV PreMIT Study. Efficacy of maternal tenofovir disoproxil fumarate in interrupting mother-to-infant transmission of hepatitis B virus. Hepatology. 2015 Aug; 62(2):375-86.

Abstract

Published on: 
Aug-2015

Sun, 30 Aug 2015

Aayushi Pratap
htmetro@hindustantimes.com

Fellow patients to share rare drug with Pakistan teenager

A group of patients, who attended a gathering on Wilson’s Disease at the Tata Memorial Hospital, have volunteered to give her (Saba Ahmed) the tablets after learning about her struggles.
DR ABHA NAGRAL

MUMBAI: Doctors at Jaslok Hospital, Peddar Road, will finally be able to give Pakistan citizen Saba Ahmed a new drug after she was unable to tolerate the standard drug given to most Wilson’s Disease patients.

Source/ Reference : http://timesofindia.indiatimes.com/city/mumbai/Pak-girls-health-improvin...
TNN | Aug 30, 2015
Mumbai: Saba Ahmed, the 15-year-old Pakistani girl who was rushed to Mumbai due to complications of a rare genetic disorder, was well enough within a week to attend a support group meeting on Saturday.

Ordinary Mumbaikars raised over Rs 3.5 lakh through a crowd-funding effort to help the teenager fly into Mumbai last week from Karachi for treatment of Wilson's Disease. Her mother Nazia said, "We found out she had Wilson's disease 18 months ago. When doctors back home told me that Saba would never again speak or walk, we came to Mumbai."

http://www.ncbi.nlm.nih.gov/pubmed/25651487

.- neonatal cholestasis

Jensen M, Abu-El-Haija M, Bishop W, Rahhal RM. Difficulty Achieving Vitamin D Sufficiency With High-Dose Oral Repletion Therapy in Infants With Cholestasis. J Pediatr Gastroenterol Nutr. 2015 Aug; 61(2):187-9.

Abstract

OBJECTIVES:
Oral high-dose repletion vitamin D therapy, also known as stoss therapy, can be effective in the treatment of nutritional vitamin D deficiency rickets in infants and young children without liver disease and in patients with cystic fibrosis. There is no literature about this approach in infants with new-onset cholestasis.

METHODS:

Published on: 
Aug-2015

http://www.ncbi.nlm.nih.gov/pubmed/26043290

Gangarapu V, Ince AT, Baysal B, Kayar Y, Kılıç U, Gök Ö, Uysal Ö, Şenturk H. Efficacy of rifaximin on circulating endotoxins and cytokines in patients with nonalcoholic fatty liver disease. Eur J Gastroenterol Hepatol. 2015 Jul;27(7):840-5.

Abstract

OBJECTIVE:
Recent studies have suggested that endotoxin-induced cytokines play an important role in nonalcoholic fatty liver disease (NAFLD). Rifaximin is a nonabsorbable antibiotic that might act on Gram-negative bacteria, thereby inhibiting endotoxin proinflammatory cytokine production in patients with NAFLD. Our aim was to investigate the efficacy of rifaximin on NAFLD.

METHODS:

Published on: 
Jul-2015

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