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4篇 您的检索式：作者名="SEEMA ALAM"

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		题名	作者	年代	出处	被引量
	1	Recent updates on progressive familial intrahepatic cholestasis types 1, 2 and 3: Outcome and therapeutic strategies显示文摘Recent evidence points towards the role of genotype to understand the phenotype,predict the natural course and long term outcome of patients with progressive familial intrahepatic cholestasis(PFIC).Expanded role of the heterozygous transporter defects presenting late needs to be suspected and identified.Treatment of pruritus,nutritional rehabilitation,prevention of fibrosis progression and liver transplantation(LT)in those with end stage liver disease form the crux of the treatment.LT in PFIC has its own unique issues like high rates of intractable diarrhoea,growth failure;steatohepatitis and graft failure in PFIC1 and antibody-mediated bile salt export pump deficiency in PFIC2.Drugs inhibiting apical sodium-dependent bile transporter and adenovirus-associated vector mediated gene therapy hold promise for future.	Seema Alam Bikrant Bihari Lal	2022	World Journal of Hepatology2022，14，1：	1
	2	Antibiotic associated diarrhea in children Indian显示文摘	SEEMA ALAM MUDASIR MUSHTAQ	2009	Pediatrics2009，46，17：	1
	3	An unusual bioactive oleanane triterpenoid from Rhododendron campanulatum D.Don显示文摘不平常的 oleanane triterpene (1 ) 从杜鹃花属 campanulatum 的天线部分被孤立。混合物显示出突出的抗菌剂和 immunomodulatory 活动。混合物的结构被分光镜的数据包括 1D 和 2D NMR 决定光谱分析。	Mudasir Ahmad Tantry Reehana Khan Seema Akbar Abdul Rouf Dar Abdul Sami Shawl Mohammad Sarwar Alam	2011	Chinese Chemical Letters2011，22，5：	1
	4	Ductal paucity and Warkany syndrome in a patient with congenital extrahepatic portocaval shunt显示文摘An eleven-year-old clinically dysmorphic and devel-opmentally retarded male child presenting with com-plaints of 5 episodes of recurrent cholestatic jaundice since 3 years of age was evaluated. Imaging revealed features consistent with congenital extrahepatic porto-caval shunt(Abernethy type 1b), multiple regenerative liver nodules and intrahepatic biliary radical dilatation. The presence of ductal paucity and trisomy 8 were con-firmed on liver biopsy and karyotyping. The explanation for unusual and previously unreported features in the present case has been proposed.	Vikrant Sood Rajeev Khanna Seema Alam Dinesh Rawat Shorav Bhatnagar Archana Rastogi	2014	World Journal of Hepatology2014，6，5：	0

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