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A case of congenital generalized lipodystrophy: metabolic effects of four dietary regimens. Lack of association of CGL with polymorphism in the lamin A/C Gene
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Published in: | Clinical endocrinology (Oxford) 2001-03, Vol.54 (3), p.412-414 |
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Main Authors: | , , , , , , , , |
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container_end_page | 414 |
container_issue | 3 |
container_start_page | 412 |
container_title | Clinical endocrinology (Oxford) |
container_volume | 54 |
creator | Kazlauskaite, Rasa Santomauro, Ana T. Goldman, Jayme Silver, Kristi Snitker, Soren Beamer, Brock A. Yen, Chung-Jen Shuldiner, Alan R. Wajchenberg, Bernardo L. |
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doi_str_mv | 10.1046/j.1365-2265.2001.1216c.x |
format | article |
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Lack of association of CGL with polymorphism in the lamin A/C Gene</title><title>Clinical endocrinology (Oxford)</title><addtitle>Clin Endocrinol (Oxf)</addtitle><subject>Adult</subject><subject>Female</subject><subject>Humans</subject><subject>Lamin Type A</subject><subject>Lamins</subject><subject>Lipodystrophy - congenital</subject><subject>Lipodystrophy - diet therapy</subject><subject>Lipodystrophy - genetics</subject><subject>Nuclear Proteins - genetics</subject><subject>Polymorphism, Genetic</subject><subject>Receptors, Adrenergic, beta - genetics</subject><subject>Receptors, Cytoplasmic and Nuclear - genetics</subject><subject>Transcription Factors - genetics</subject><issn>0300-0664</issn><issn>1365-2265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNqNkc-O0zAQxiMEYsvCKyCLe7L-UzsOB6QqWrorVYuQQBwtx5m07iZxsNPdlofhWdehVRdunGasb-Y3M_6SBBGcETwXV9uMMMFTSgXPKMYkI5QIk-1fJLOz8DKZYYZxioWYXyRvQthijLnE-evkghBaSFzIWfJ7gYwOgFyDjOvX0NtRtyhG8Lq1v6BGrR1cfQijd8Pm8BF1MOrKtdYgaBowY5haG7fzqLZR8gfkYW076EOGVtrcT7IOwRmrR-v66VkuV-jRjhs0uPbQOT9sbOiQ7dG4AdTqLmaLqxIt4xJvk1eNbgO8O8XL5Pvn62_lTbr6srwtF6vUcMzLFGRFtCFENzU1OReGSFrVWs6ZYDklIArQMQMhOeEmKkVOi3mloSFC01yyy-TTkTvsqg5qA_0Y71eDt108STlt1b9Kbzdq7R4UYwUuGIuADyeAdz93EEa1jX_Sx50VKWQuOaVFLJLHIuNdCB6a8wCC1WSs2qrJPzX5pyZj1R9j1T62vv97wefGk5PPFzzaFg7_DVbl9d2UlhGQHgE2jLA_A7S_VyJnOVc_7paqLOVXesO5kuwJxSrEcw</recordid><startdate>200103</startdate><enddate>200103</enddate><creator>Kazlauskaite, Rasa</creator><creator>Santomauro, Ana T.</creator><creator>Goldman, Jayme</creator><creator>Silver, Kristi</creator><creator>Snitker, Soren</creator><creator>Beamer, Brock A.</creator><creator>Yen, Chung-Jen</creator><creator>Shuldiner, Alan R.</creator><creator>Wajchenberg, Bernardo L.</creator><general>Blackwell Science Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>5PM</scope></search><sort><creationdate>200103</creationdate><title>A case of congenital generalized lipodystrophy: metabolic effects of four dietary regimens. Lack of association of CGL with polymorphism in the lamin A/C Gene</title><author>Kazlauskaite, Rasa ; Santomauro, Ana T. ; Goldman, Jayme ; Silver, Kristi ; Snitker, Soren ; Beamer, Brock A. ; Yen, Chung-Jen ; Shuldiner, Alan R. ; Wajchenberg, Bernardo L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c505C-e8b1ac11afd2c756c182bda84363721e69ea637e68515cbda97294baef16a2783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Adult</topic><topic>Female</topic><topic>Humans</topic><topic>Lamin Type A</topic><topic>Lamins</topic><topic>Lipodystrophy - congenital</topic><topic>Lipodystrophy - diet therapy</topic><topic>Lipodystrophy - genetics</topic><topic>Nuclear Proteins - genetics</topic><topic>Polymorphism, Genetic</topic><topic>Receptors, Adrenergic, beta - genetics</topic><topic>Receptors, Cytoplasmic and Nuclear - genetics</topic><topic>Transcription Factors - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kazlauskaite, Rasa</creatorcontrib><creatorcontrib>Santomauro, Ana T.</creatorcontrib><creatorcontrib>Goldman, Jayme</creatorcontrib><creatorcontrib>Silver, Kristi</creatorcontrib><creatorcontrib>Snitker, Soren</creatorcontrib><creatorcontrib>Beamer, Brock A.</creatorcontrib><creatorcontrib>Yen, Chung-Jen</creatorcontrib><creatorcontrib>Shuldiner, Alan R.</creatorcontrib><creatorcontrib>Wajchenberg, Bernardo L.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical endocrinology (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kazlauskaite, Rasa</au><au>Santomauro, Ana T.</au><au>Goldman, Jayme</au><au>Silver, Kristi</au><au>Snitker, Soren</au><au>Beamer, Brock A.</au><au>Yen, Chung-Jen</au><au>Shuldiner, Alan R.</au><au>Wajchenberg, Bernardo L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A case of congenital generalized lipodystrophy: metabolic effects of four dietary regimens. 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ispartof | Clinical endocrinology (Oxford), 2001-03, Vol.54 (3), p.412-414 |
issn | 0300-0664 1365-2265 |
language | eng |
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source | Wiley |
subjects | Adult Female Humans Lamin Type A Lamins Lipodystrophy - congenital Lipodystrophy - diet therapy Lipodystrophy - genetics Nuclear Proteins - genetics Polymorphism, Genetic Receptors, Adrenergic, beta - genetics Receptors, Cytoplasmic and Nuclear - genetics Transcription Factors - genetics |
title | A case of congenital generalized lipodystrophy: metabolic effects of four dietary regimens. Lack of association of CGL with polymorphism in the lamin A/C Gene |
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