Tetrahydrobiopterin therapy vs phenylalanine-restricted diet: Impact on growth in PKU

Treatment of phenylketonuria based upon strict vegetarian diets, with very low phenylalanine intake and supplemented by phenylalanine-free formula, has proven to be effective in preventing the development of long-term neurological sequelae due to phenylalanine accumulation. On the other hand, such d...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Molecular genetics and metabolism 2013-08, Vol.109 (4), p.331-338
Hauptverfasser: Aldámiz-Echevarría, Luis, Bueno, María A., Couce, María L., Lage, Sergio, Dalmau, Jaime, Vitoria, Isidro, Andrade, Fernando, Llarena, Marta, Blasco, Javier, Alcalde, Carlos, Gil, David, García, María C., González-Lamuño, Domingo, Ruiz, Mónica, Ruiz, María A., González, David, Sánchez-Valverde, Felix
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 338
container_issue 4
container_start_page 331
container_title Molecular genetics and metabolism
container_volume 109
creator Aldámiz-Echevarría, Luis
Bueno, María A.
Couce, María L.
Lage, Sergio
Dalmau, Jaime
Vitoria, Isidro
Andrade, Fernando
Llarena, Marta
Blasco, Javier
Alcalde, Carlos
Gil, David
García, María C.
González-Lamuño, Domingo
Ruiz, Mónica
Ruiz, María A.
González, David
Sánchez-Valverde, Felix
description Treatment of phenylketonuria based upon strict vegetarian diets, with very low phenylalanine intake and supplemented by phenylalanine-free formula, has proven to be effective in preventing the development of long-term neurological sequelae due to phenylalanine accumulation. On the other hand, such diets have occasionally been reported to hinder normal development, some individuals presenting with growth retardation. Tetrahydrobiopterin therapy has opened up new treatment options for a significant proportion of phenylketonuric patients, enabling them to eat normal diets and be freed from the need to take synthetic supplements. However, little is known about how this therapy affects their physical development. We conducted a retrospective longitudinal study examining anthropometric characteristics (height, weight, body mass index and growth speed Z-scores) in a cohort of phenylketonuric patients on tetrahydrobiopterin therapy (38 subjects) comparing their characteristics with those of a group of phenylketonuric patients on phenylalanine-restricted diets (76 subjects). Nutritional issues were also considered, to further explore the possibility of higher natural protein intake being associated with better physical development. Data were collected every six months over two different periods of time (two or five years). No improvement was observed in the aforementioned anthropometric variables in the cohort on tetrahydrobiopterin therapy, from prior to starting treatment to when they had been taking the drug for two or five years. Rather, in almost all cases there was a fall in the mean Z-score for the variables during these periods, although the changes were not significant in any case. Further, we found no statistically differences between the two groups at any considered time point. Growth impairment was also noted in the phenylketonuric patients on low-phenylalanine diets. Individuals on tetrahydrobiopterin therapy increased their natural protein intake and, in some instances, this treatment enabled individuals to eat normal diets, with protein intake meeting RDAs. No association was found, however, between higher protein intake and growth. Our study identified growth impairment in patients with phenylketonuria on tetrahydrobiopterin, despite higher intakes of natural proteins. In fact, individuals undergoing long-term tetrahydrobiopterin treatment seemed to achieve similar developmental outcomes to those attained by individuals on more restricted diets. •BH
doi_str_mv 10.1016/j.ymgme.2013.05.017
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1415604817</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1096719213001832</els_id><sourcerecordid>1415604817</sourcerecordid><originalsourceid>FETCH-LOGICAL-c359t-b1ee94552271ebb28dc7fdc4475d77c51d4ea2de57d7dcacbd977c3974d6facb3</originalsourceid><addsrcrecordid>eNp9UMtOwzAQtBCIR-ELkFCOXBK8SRw3SBwQ4iUqwaE9W469Ia6aB7ZblL_HpcCR0z40szM7hJwDTYBCcbVMxva9xSSlkCWUJRT4HjkGWhYxT2mx_9tDmR6RE-eWlAKwMj8kR2k2BZqm_Jgs5uitbEZt-8r0g0drusg3aOUwRhsXDQ1240quZGc6jC06b43yqCNt0F9Hz-0glY_6Lnq3_advosB-e1mckoNarhye_dQJWTzcz--e4tnr4_Pd7SxWGSt9XAFimTMWnABWVTrVitda5TlnmnPFQOcoU42Ma66VVJUuwzorea6LOozZhFzu7g62_1gHc6I1TuEq2MV-7QTkwAqaT4EHaLaDKts7Z7EWgzWttKMAKrZ5iqX4zlNs8xSUCfrNuvgRWFct6j_Ob4ABcLMDYHhzY9AKpwx2CrWxqLzQvflX4AtzUYmu</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1415604817</pqid></control><display><type>article</type><title>Tetrahydrobiopterin therapy vs phenylalanine-restricted diet: Impact on growth in PKU</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><creator>Aldámiz-Echevarría, Luis ; Bueno, María A. ; Couce, María L. ; Lage, Sergio ; Dalmau, Jaime ; Vitoria, Isidro ; Andrade, Fernando ; Llarena, Marta ; Blasco, Javier ; Alcalde, Carlos ; Gil, David ; García, María C. ; González-Lamuño, Domingo ; Ruiz, Mónica ; Ruiz, María A. ; González, David ; Sánchez-Valverde, Felix</creator><creatorcontrib>Aldámiz-Echevarría, Luis ; Bueno, María A. ; Couce, María L. ; Lage, Sergio ; Dalmau, Jaime ; Vitoria, Isidro ; Andrade, Fernando ; Llarena, Marta ; Blasco, Javier ; Alcalde, Carlos ; Gil, David ; García, María C. ; González-Lamuño, Domingo ; Ruiz, Mónica ; Ruiz, María A. ; González, David ; Sánchez-Valverde, Felix</creatorcontrib><description>Treatment of phenylketonuria based upon strict vegetarian diets, with very low phenylalanine intake and supplemented by phenylalanine-free formula, has proven to be effective in preventing the development of long-term neurological sequelae due to phenylalanine accumulation. On the other hand, such diets have occasionally been reported to hinder normal development, some individuals presenting with growth retardation. Tetrahydrobiopterin therapy has opened up new treatment options for a significant proportion of phenylketonuric patients, enabling them to eat normal diets and be freed from the need to take synthetic supplements. However, little is known about how this therapy affects their physical development. We conducted a retrospective longitudinal study examining anthropometric characteristics (height, weight, body mass index and growth speed Z-scores) in a cohort of phenylketonuric patients on tetrahydrobiopterin therapy (38 subjects) comparing their characteristics with those of a group of phenylketonuric patients on phenylalanine-restricted diets (76 subjects). Nutritional issues were also considered, to further explore the possibility of higher natural protein intake being associated with better physical development. Data were collected every six months over two different periods of time (two or five years). No improvement was observed in the aforementioned anthropometric variables in the cohort on tetrahydrobiopterin therapy, from prior to starting treatment to when they had been taking the drug for two or five years. Rather, in almost all cases there was a fall in the mean Z-score for the variables during these periods, although the changes were not significant in any case. Further, we found no statistically differences between the two groups at any considered time point. Growth impairment was also noted in the phenylketonuric patients on low-phenylalanine diets. Individuals on tetrahydrobiopterin therapy increased their natural protein intake and, in some instances, this treatment enabled individuals to eat normal diets, with protein intake meeting RDAs. No association was found, however, between higher protein intake and growth. Our study identified growth impairment in patients with phenylketonuria on tetrahydrobiopterin, despite higher intakes of natural proteins. In fact, individuals undergoing long-term tetrahydrobiopterin treatment seemed to achieve similar developmental outcomes to those attained by individuals on more restricted diets. •BH4 therapy enables a significant proportion of PKU patients to eat normal diets.•We examined anthropometrics in a cohort of PKU patients on BH4.•No improvement was observed in anthropometric variables in the BH4 cohort.•Despite consuming natural proteins, BH4 patients did not attain better growth.</description><identifier>ISSN: 1096-7192</identifier><identifier>EISSN: 1096-7206</identifier><identifier>DOI: 10.1016/j.ymgme.2013.05.017</identifier><identifier>PMID: 23810227</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Biopterins - administration &amp; dosage ; Biopterins - analogs &amp; derivatives ; Body Composition - drug effects ; Body Height - drug effects ; Body Mass Index ; Body Weight - drug effects ; Diet ; Follow-Up Studies ; Growth ; Humans ; Phenylalanine - administration &amp; dosage ; Phenylalanine - metabolism ; Phenylketonuria ; Phenylketonurias - diet therapy ; Phenylketonurias - pathology ; Tetrahydrobiopterin</subject><ispartof>Molecular genetics and metabolism, 2013-08, Vol.109 (4), p.331-338</ispartof><rights>2013 Elsevier Inc.</rights><rights>Copyright © 2013 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c359t-b1ee94552271ebb28dc7fdc4475d77c51d4ea2de57d7dcacbd977c3974d6facb3</citedby><cites>FETCH-LOGICAL-c359t-b1ee94552271ebb28dc7fdc4475d77c51d4ea2de57d7dcacbd977c3974d6facb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ymgme.2013.05.017$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27926,27927,45997</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23810227$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Aldámiz-Echevarría, Luis</creatorcontrib><creatorcontrib>Bueno, María A.</creatorcontrib><creatorcontrib>Couce, María L.</creatorcontrib><creatorcontrib>Lage, Sergio</creatorcontrib><creatorcontrib>Dalmau, Jaime</creatorcontrib><creatorcontrib>Vitoria, Isidro</creatorcontrib><creatorcontrib>Andrade, Fernando</creatorcontrib><creatorcontrib>Llarena, Marta</creatorcontrib><creatorcontrib>Blasco, Javier</creatorcontrib><creatorcontrib>Alcalde, Carlos</creatorcontrib><creatorcontrib>Gil, David</creatorcontrib><creatorcontrib>García, María C.</creatorcontrib><creatorcontrib>González-Lamuño, Domingo</creatorcontrib><creatorcontrib>Ruiz, Mónica</creatorcontrib><creatorcontrib>Ruiz, María A.</creatorcontrib><creatorcontrib>González, David</creatorcontrib><creatorcontrib>Sánchez-Valverde, Felix</creatorcontrib><title>Tetrahydrobiopterin therapy vs phenylalanine-restricted diet: Impact on growth in PKU</title><title>Molecular genetics and metabolism</title><addtitle>Mol Genet Metab</addtitle><description>Treatment of phenylketonuria based upon strict vegetarian diets, with very low phenylalanine intake and supplemented by phenylalanine-free formula, has proven to be effective in preventing the development of long-term neurological sequelae due to phenylalanine accumulation. On the other hand, such diets have occasionally been reported to hinder normal development, some individuals presenting with growth retardation. Tetrahydrobiopterin therapy has opened up new treatment options for a significant proportion of phenylketonuric patients, enabling them to eat normal diets and be freed from the need to take synthetic supplements. However, little is known about how this therapy affects their physical development. We conducted a retrospective longitudinal study examining anthropometric characteristics (height, weight, body mass index and growth speed Z-scores) in a cohort of phenylketonuric patients on tetrahydrobiopterin therapy (38 subjects) comparing their characteristics with those of a group of phenylketonuric patients on phenylalanine-restricted diets (76 subjects). Nutritional issues were also considered, to further explore the possibility of higher natural protein intake being associated with better physical development. Data were collected every six months over two different periods of time (two or five years). No improvement was observed in the aforementioned anthropometric variables in the cohort on tetrahydrobiopterin therapy, from prior to starting treatment to when they had been taking the drug for two or five years. Rather, in almost all cases there was a fall in the mean Z-score for the variables during these periods, although the changes were not significant in any case. Further, we found no statistically differences between the two groups at any considered time point. Growth impairment was also noted in the phenylketonuric patients on low-phenylalanine diets. Individuals on tetrahydrobiopterin therapy increased their natural protein intake and, in some instances, this treatment enabled individuals to eat normal diets, with protein intake meeting RDAs. No association was found, however, between higher protein intake and growth. Our study identified growth impairment in patients with phenylketonuria on tetrahydrobiopterin, despite higher intakes of natural proteins. In fact, individuals undergoing long-term tetrahydrobiopterin treatment seemed to achieve similar developmental outcomes to those attained by individuals on more restricted diets. •BH4 therapy enables a significant proportion of PKU patients to eat normal diets.•We examined anthropometrics in a cohort of PKU patients on BH4.•No improvement was observed in anthropometric variables in the BH4 cohort.•Despite consuming natural proteins, BH4 patients did not attain better growth.</description><subject>Biopterins - administration &amp; dosage</subject><subject>Biopterins - analogs &amp; derivatives</subject><subject>Body Composition - drug effects</subject><subject>Body Height - drug effects</subject><subject>Body Mass Index</subject><subject>Body Weight - drug effects</subject><subject>Diet</subject><subject>Follow-Up Studies</subject><subject>Growth</subject><subject>Humans</subject><subject>Phenylalanine - administration &amp; dosage</subject><subject>Phenylalanine - metabolism</subject><subject>Phenylketonuria</subject><subject>Phenylketonurias - diet therapy</subject><subject>Phenylketonurias - pathology</subject><subject>Tetrahydrobiopterin</subject><issn>1096-7192</issn><issn>1096-7206</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UMtOwzAQtBCIR-ELkFCOXBK8SRw3SBwQ4iUqwaE9W469Ia6aB7ZblL_HpcCR0z40szM7hJwDTYBCcbVMxva9xSSlkCWUJRT4HjkGWhYxT2mx_9tDmR6RE-eWlAKwMj8kR2k2BZqm_Jgs5uitbEZt-8r0g0drusg3aOUwRhsXDQ1240quZGc6jC06b43yqCNt0F9Hz-0glY_6Lnq3_advosB-e1mckoNarhye_dQJWTzcz--e4tnr4_Pd7SxWGSt9XAFimTMWnABWVTrVitda5TlnmnPFQOcoU42Ma66VVJUuwzorea6LOozZhFzu7g62_1gHc6I1TuEq2MV-7QTkwAqaT4EHaLaDKts7Z7EWgzWttKMAKrZ5iqX4zlNs8xSUCfrNuvgRWFct6j_Ob4ABcLMDYHhzY9AKpwx2CrWxqLzQvflX4AtzUYmu</recordid><startdate>201308</startdate><enddate>201308</enddate><creator>Aldámiz-Echevarría, Luis</creator><creator>Bueno, María A.</creator><creator>Couce, María L.</creator><creator>Lage, Sergio</creator><creator>Dalmau, Jaime</creator><creator>Vitoria, Isidro</creator><creator>Andrade, Fernando</creator><creator>Llarena, Marta</creator><creator>Blasco, Javier</creator><creator>Alcalde, Carlos</creator><creator>Gil, David</creator><creator>García, María C.</creator><creator>González-Lamuño, Domingo</creator><creator>Ruiz, Mónica</creator><creator>Ruiz, María A.</creator><creator>González, David</creator><creator>Sánchez-Valverde, Felix</creator><general>Elsevier Inc</general><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>7X8</scope></search><sort><creationdate>201308</creationdate><title>Tetrahydrobiopterin therapy vs phenylalanine-restricted diet: Impact on growth in PKU</title><author>Aldámiz-Echevarría, Luis ; Bueno, María A. ; Couce, María L. ; Lage, Sergio ; Dalmau, Jaime ; Vitoria, Isidro ; Andrade, Fernando ; Llarena, Marta ; Blasco, Javier ; Alcalde, Carlos ; Gil, David ; García, María C. ; González-Lamuño, Domingo ; Ruiz, Mónica ; Ruiz, María A. ; González, David ; Sánchez-Valverde, Felix</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-b1ee94552271ebb28dc7fdc4475d77c51d4ea2de57d7dcacbd977c3974d6facb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Biopterins - administration &amp; dosage</topic><topic>Biopterins - analogs &amp; derivatives</topic><topic>Body Composition - drug effects</topic><topic>Body Height - drug effects</topic><topic>Body Mass Index</topic><topic>Body Weight - drug effects</topic><topic>Diet</topic><topic>Follow-Up Studies</topic><topic>Growth</topic><topic>Humans</topic><topic>Phenylalanine - administration &amp; dosage</topic><topic>Phenylalanine - metabolism</topic><topic>Phenylketonuria</topic><topic>Phenylketonurias - diet therapy</topic><topic>Phenylketonurias - pathology</topic><topic>Tetrahydrobiopterin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aldámiz-Echevarría, Luis</creatorcontrib><creatorcontrib>Bueno, María A.</creatorcontrib><creatorcontrib>Couce, María L.</creatorcontrib><creatorcontrib>Lage, Sergio</creatorcontrib><creatorcontrib>Dalmau, Jaime</creatorcontrib><creatorcontrib>Vitoria, Isidro</creatorcontrib><creatorcontrib>Andrade, Fernando</creatorcontrib><creatorcontrib>Llarena, Marta</creatorcontrib><creatorcontrib>Blasco, Javier</creatorcontrib><creatorcontrib>Alcalde, Carlos</creatorcontrib><creatorcontrib>Gil, David</creatorcontrib><creatorcontrib>García, María C.</creatorcontrib><creatorcontrib>González-Lamuño, Domingo</creatorcontrib><creatorcontrib>Ruiz, Mónica</creatorcontrib><creatorcontrib>Ruiz, María A.</creatorcontrib><creatorcontrib>González, David</creatorcontrib><creatorcontrib>Sánchez-Valverde, Felix</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular genetics and metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aldámiz-Echevarría, Luis</au><au>Bueno, María A.</au><au>Couce, María L.</au><au>Lage, Sergio</au><au>Dalmau, Jaime</au><au>Vitoria, Isidro</au><au>Andrade, Fernando</au><au>Llarena, Marta</au><au>Blasco, Javier</au><au>Alcalde, Carlos</au><au>Gil, David</au><au>García, María C.</au><au>González-Lamuño, Domingo</au><au>Ruiz, Mónica</au><au>Ruiz, María A.</au><au>González, David</au><au>Sánchez-Valverde, Felix</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tetrahydrobiopterin therapy vs phenylalanine-restricted diet: Impact on growth in PKU</atitle><jtitle>Molecular genetics and metabolism</jtitle><addtitle>Mol Genet Metab</addtitle><date>2013-08</date><risdate>2013</risdate><volume>109</volume><issue>4</issue><spage>331</spage><epage>338</epage><pages>331-338</pages><issn>1096-7192</issn><eissn>1096-7206</eissn><abstract>Treatment of phenylketonuria based upon strict vegetarian diets, with very low phenylalanine intake and supplemented by phenylalanine-free formula, has proven to be effective in preventing the development of long-term neurological sequelae due to phenylalanine accumulation. On the other hand, such diets have occasionally been reported to hinder normal development, some individuals presenting with growth retardation. Tetrahydrobiopterin therapy has opened up new treatment options for a significant proportion of phenylketonuric patients, enabling them to eat normal diets and be freed from the need to take synthetic supplements. However, little is known about how this therapy affects their physical development. We conducted a retrospective longitudinal study examining anthropometric characteristics (height, weight, body mass index and growth speed Z-scores) in a cohort of phenylketonuric patients on tetrahydrobiopterin therapy (38 subjects) comparing their characteristics with those of a group of phenylketonuric patients on phenylalanine-restricted diets (76 subjects). Nutritional issues were also considered, to further explore the possibility of higher natural protein intake being associated with better physical development. Data were collected every six months over two different periods of time (two or five years). No improvement was observed in the aforementioned anthropometric variables in the cohort on tetrahydrobiopterin therapy, from prior to starting treatment to when they had been taking the drug for two or five years. Rather, in almost all cases there was a fall in the mean Z-score for the variables during these periods, although the changes were not significant in any case. Further, we found no statistically differences between the two groups at any considered time point. Growth impairment was also noted in the phenylketonuric patients on low-phenylalanine diets. Individuals on tetrahydrobiopterin therapy increased their natural protein intake and, in some instances, this treatment enabled individuals to eat normal diets, with protein intake meeting RDAs. No association was found, however, between higher protein intake and growth. Our study identified growth impairment in patients with phenylketonuria on tetrahydrobiopterin, despite higher intakes of natural proteins. In fact, individuals undergoing long-term tetrahydrobiopterin treatment seemed to achieve similar developmental outcomes to those attained by individuals on more restricted diets. •BH4 therapy enables a significant proportion of PKU patients to eat normal diets.•We examined anthropometrics in a cohort of PKU patients on BH4.•No improvement was observed in anthropometric variables in the BH4 cohort.•Despite consuming natural proteins, BH4 patients did not attain better growth.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>23810227</pmid><doi>10.1016/j.ymgme.2013.05.017</doi><tpages>8</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1096-7192
ispartof Molecular genetics and metabolism, 2013-08, Vol.109 (4), p.331-338
issn 1096-7192
1096-7206
language eng
recordid cdi_proquest_miscellaneous_1415604817
source MEDLINE; Elsevier ScienceDirect Journals Complete
subjects Biopterins - administration & dosage
Biopterins - analogs & derivatives
Body Composition - drug effects
Body Height - drug effects
Body Mass Index
Body Weight - drug effects
Diet
Follow-Up Studies
Growth
Humans
Phenylalanine - administration & dosage
Phenylalanine - metabolism
Phenylketonuria
Phenylketonurias - diet therapy
Phenylketonurias - pathology
Tetrahydrobiopterin
title Tetrahydrobiopterin therapy vs phenylalanine-restricted diet: Impact on growth in PKU
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T07%3A06%3A32IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Tetrahydrobiopterin%20therapy%20vs%20phenylalanine-restricted%20diet:%20Impact%20on%20growth%20in%20PKU&rft.jtitle=Molecular%20genetics%20and%20metabolism&rft.au=Ald%C3%A1miz-Echevarr%C3%ADa,%20Luis&rft.date=2013-08&rft.volume=109&rft.issue=4&rft.spage=331&rft.epage=338&rft.pages=331-338&rft.issn=1096-7192&rft.eissn=1096-7206&rft_id=info:doi/10.1016/j.ymgme.2013.05.017&rft_dat=%3Cproquest_cross%3E1415604817%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1415604817&rft_id=info:pmid/23810227&rft_els_id=S1096719213001832&rfr_iscdi=true