Treatment Of Phenylketonuria With Bh4 - EP3138566

The patent EP3138566 was granted to Biomarin Pharmaceutical on Jan 26, 2022. The application was originally filed on Nov 17, 2004 under application number EP16178739A. The patent is currently recorded with a legal status of "Revoked".

EP3138566

BIOMARIN PHARMACEUTICAL
Application Number
EP16178739A
Filing Date
Nov 17, 2004
Status
Revoked
Jun 7, 2024
Grant Date
Jan 26, 2022
External Links
Slate, Register, Google Patents

Patent Summary

Patent Family

Patent Family

Patent Oppositions (3)

Patent oppositions filed by competitors challenge the validity of a granted patent. These oppositions are typically based on claims of prior art, lack of novelty, or non-obviousness. They are a key part of the process for determining a patent's strength and enforceability.

CompanyOpposition DateRepresentativeOpposition Status

Get instant alerts for new oppositions and patent status changes

DIPHARMAOct 26, 2022ELKINGTON AND FIFEWITHDRAWN
TOBIO NOVELFARMA ILAC SAN VE TICOct 12, 2022BULUTADMISSIBLE
STADA ARZNEIMITTELOct 6, 2022HAMM & WITTKOPPADMISSIBLE

Patent Citations (55) New

Patent citations refer to prior patents cited during different phases such as opposition or international search.

Citation PhasePublication NumberPublication Link
DESCRIPTIONUS20030520377-
DESCRIPTIONCA2420374
DESCRIPTIONEP0079574
DESCRIPTIONEP0191335
DESCRIPTIONUS2002076782
DESCRIPTIONUS2002106645
DESCRIPTIONUS2002187958
DESCRIPTIONUS2003032616
DESCRIPTIONUS2541717
DESCRIPTIONUS2601215
DESCRIPTIONUS2603643
DESCRIPTIONUS2955110
DESCRIPTIONUS3505329
DESCRIPTIONUS4252822
DESCRIPTIONUS4371514
DESCRIPTIONUS4540783
DESCRIPTIONUS4550109
DESCRIPTIONUS4587340
DESCRIPTIONUS4595752
DESCRIPTIONUS4649197
DESCRIPTIONUS4665182
DESCRIPTIONUS4701455
DESCRIPTIONUS4713454
DESCRIPTIONUS4752573
DESCRIPTIONUS4758571
DESCRIPTIONUS4774244
DESCRIPTIONUS4920122
DESCRIPTIONUS4937342
DESCRIPTIONUS5037981
DESCRIPTIONUS5198547
DESCRIPTIONUS5350851
DESCRIPTIONUS5401844
DESCRIPTIONUS5698408
DESCRIPTIONUS5753656
DESCRIPTIONUS5874433
DESCRIPTIONUS5902810
DESCRIPTIONUS5922713
DESCRIPTIONUS5945452
DESCRIPTIONUS6011040
DESCRIPTIONUS6162806
DESCRIPTIONUS6271374
DESCRIPTIONUS6274581
DESCRIPTIONUS6410535
DESCRIPTIONUS6441038
DESCRIPTIONUS6441168
DESCRIPTIONUS6506422
DESCRIPTIONUS6544994
DESCRIPTIONUS6596721
EXAMINATIONEP0153696
EXAMINATIONEP0191335
EXAMINATIONWO2006004719
OPPOSITIONEP0153696
OPPOSITIONEP0191335
OPPOSITIONWO2005065018
OPPOSITIONWO2006004719

Non-Patent Literature (NPL) Citations (81) New

NPL citations refer to non-patent references such as research papers, articles, or other publications cited during examination or opposition phases.

Citation PhaseReference TextLink
DESCRIPTION- BEMEGGAR; BLAU, MOL. GENET. METABOL., (2002), vol. 77, pages 304 - 313-
DESCRIPTION- BERNEGGAR; BLAU, MOL. GENET. METABOL., (2002), vol. 77, pages 304 - 313-
DESCRIPTION- BLAU ET AL., "Disorders of tetrahydrobiopterin and related biogenic amines", BLAU ET AL., SCRIVER CR, BEAUDET AL, SLY WS, VALLE D, CHILDS B, VOGELSTEIN B, The Metabolic and Molecular Bases of Inherited Disease, 8th ed., NEW YORK: MCGRAW-HILL, (2001), pages 1275 - 1776-
DESCRIPTION- CHRISTENSEN ET AL., GENE THERAPY, (2000), vol. 7, pages 1971 - 1978-
DESCRIPTION- CHRISTENSEN ET AL., MOL. GENT. ANDMETABOL., (2002), vol. 76, pages 313 - 318-
DESCRIPTION- D'AGOSTINO, N. ENGL. J. MED., (2003), vol. 348, no. 17, pages 1723 - 1724-
DESCRIPTION- DAVIS ET AL., EUR. J. BIOCHEM., (1988), vol. 173, pages 345 - 351-
DESCRIPTION- HANLEY, N. ENGL. J. MED, (2003), vol. 348, no. 17, page 1723-
DESCRIPTION- HETEROCYCLES, (1985), vol. 23, no. 12, pages 3115 - 3120-
DESCRIPTION- J. BIOCHEM., (1985), vol. 98, pages 1341 - 1348-
DESCRIPTION- KOCH ET AL., MOL. GENET. METABOL., (2003), vol. 79, pages 110 - 113-
DESCRIPTION- KURE ET AL., J. PEDIATR., (1999), vol. 135, pages 375 - 378-
DESCRIPTION- LASSKER ET AL., J. INHERIT. METABOL. DIS., (2002), vol. 25, pages 65 - 70-
DESCRIPTION- LINDER ET AL., MOL. GENET. METAB., (2001), vol. 73, pages 104 - 106-
DESCRIPTION- LUCKE ET AL., PEDIATR. NEUROL., (2003), vol. 28, pages 228 - 230-
DESCRIPTION- MCCAMAN ET AL., J. LAB. CLIN. MED., (1962), vol. 59, pages 885 - 890-
DESCRIPTION- MUNTAU ET AL., N. ENGL. J. MED., (2002), vol. 347, no. 26-
DESCRIPTION- NIH CONSENSUS STATEMENT, (200010), vol. 17 #3-
DESCRIPTION- PAL LIU ET AL., ARTS. CELLS. BLOOD. SUBS AND IMMOB. BIOTECH., (2002), vol. 30, no. 4, pages 243 - 257-
DESCRIPTION- PONZONE ET AL., EUR. J. PEDIATR., (1993), vol. 152, pages 655 - 661-
DESCRIPTION- PONZONE ET AL., N. ENGL. J. MED, (2003), vol. 348, no. 17, pages 1722 - 1723-
DESCRIPTION- Remington's Pharmaceutical Sciences, 18th ed., MACKPUBL. CO, (1990), pages 1435 - 1712-
DESCRIPTION- SCRIVER ET AL., "Hyperphenylalaninemia: Phenylalanine Hydroxylase Deficiency", SCRIVER ET AL., SCRIVER CR, BEAUDET AL, SLY WS, VALLE D, CHILDS B, VOGELSTEIN B, The Metabolic and Molecular Bases of Inherited Disease, 8th ed., NEW YORK: MCGRAW-HILL, (2001), pages 1667 - 1724-
DESCRIPTION- SHAW ET AL., "Analytical Methods in Phenylketonuria-Clinical Biochemistry", SHAW ET AL., BICKETT ET AL., Phenylketonuria and Some Other Inborn Errors of Amino Acid Metabolism, STUTTGART, GEORG THIEM VERLAG, (1971), pages 47 - 56-
DESCRIPTION- S. MATSUURA ET AL., CHEMISTRY LETTERS, (1984), pages 735 - 738-
DESCRIPTION- SPAAPEN ET AL., MO . GENET AND METAB., (2003), vol. 78, pages 93 - 99-
DESCRIPTION- SPAAPEN ET AL., MOL. GENET. AND METABOL., (2003), vol. 78, pages 93 - 99-
DESCRIPTION- SPAAPEN ET AL., MOL. GENET. AND METABOLISM, (2003), vol. 78, pages 93 - 99-
DESCRIPTION- TREACY ET AL., PEDIAT. RES., (1997), vol. 42, pages 430 - 5-
DESCRIPTION- WEGLAGE ET AL., J. INHERIT. METAB. DIS., (2002), vol. 25, pages 321 - 322-
EXAMINATION- MOLECULAR GENETICS AND METABOLISM 20030201 US, (20030201), vol. 78, no. 2, ISSN 1096-7192, pages 93 - 99-
EXAMINATION- SPAAPEN L J M ET AL, "Tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency, state of the art", EMBASE, ELSEVIER SCIENCE PUBLISHERS, AMSTERDAM, NL, (20030201), Database accession no. EMB-2003100860-
EXAMINATION- MATSUURA S ET AL, "Highly stereoselective procedure for (6R)-tetrahydrobiopterin cofactor", CHEMISTRY LETTERS, CHEMICAL SOCIETY OF JAPAN,NIPPON KAGAKUKAI, JP, (19840101), doi:10.1246/CL.1984.735, ISSN 0366-7022, pages 735 - 738, XP003028704
OPPOSITION- Anonymous, "Biomarin Form 8-K", Washington, Washington, (20031120), pages 1 - 6, (20211210), XP055871779-
OPPOSITION- Anonymous, "Tetrahydrobiopterin Data Sheet", schircks laboratoires, (20030916), XP055973923-
OPPOSITION- Anonymous, "Tetrahydrobiopterin Tablets ", schircks laboratories, (20030315), XP055973920-
OPPOSITION- Biomarin Pharmaceutical Inc, "KUVAN Consumer Medicine Information", Medsafe, (20170113), Medsafe , URL: http://web.archive.org/web/20121014215930/http://www.medsafe.govt.nz/Consumers/cmi/k/kuvan.pdf, (19000101), XP002765924-
OPPOSITION- Blau, "Disorders of tetrahydrobiopterin and related biogenic amines", (20010101), URL: https://www.researchgate.net/profile/Beat_Thoeny/publication/233414667_Disorders_of_tetrahydrobiopterin_and_related_biogenic_amines/links/09e4150dddf878fbaf000000.pdf, (20170113), XP002765923-
OPPOSITION- Hennermann J B; Vetter B; Kulozik A E; Moench E, "Partial and total tetrahydrobiopterin-responsiveness in classical and mild phenylketonuria (PKU)", JOURNAL OF INHERITED METABOLIC DISEASE., KLUWER, DORDRECHT., NL, NL , (20020906), vol. 25, no. Suppl.1, ISSN 0141-8955, page 21, XP009184263-
OPPOSITION- Hennermann J B; Vetter B; Kulozik A E; Moench E, "Partial and total tetrahydrobiopterin-responsiveness in classical and mild phenylketonuria (PKU)", JOURNAL OF INHERITED METABOLIC DISEASE, NL , (20020906), vol. 25, no. Suppl.1, ISSN 0141-8955, page 21, XP009184263-
OPPOSITION- Kure, S. ; Hou, D.C. ; Ohura, T. ; Iwamoto, H. ; Suzuki, S. ; Sugiyama, N. ; Sakamoto, O. ; Fujii, K. ; Matsubara, Y. ; Narisawa, K., "Tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency", JOURNAL OF PEDIATRICS., MOSBY-YEAR BOOK, ST. LOUIS, MO, US, US , (19990901), vol. 135, no. 3, ISSN 0022-3476, pages 375 - 378, XP027376711-
OPPOSITION- N/a, "CHMP assessment report for Kuvan. (sapropterin)", European Medicines Agency (Ref: EMEA/604757/2008), (20080101), pages 1 - 39, European Medicines Agency (Ref: EMEA/604757/2008), (20170530), XP055376944-
OPPOSITION- Nenad Blau, Beat Thony, Richard G.H Cotton , Keith Hyland , "CHAPTER 8", Disorders Tetrahydrobiopterin and Related Biogenic Amines, (20010101), pages 1725 - 1776, XP055973896-
OPPOSITION- STEINFELD R, ET AL, "A hypothesis on the biochemical mechanism of BH4-responsiveness in phenylalanine hydroxylase deficiency", AMINO ACIDS, AU , (20030101), vol. 25, no. 1, ISSN 0939-4451, pages 63 - 68, XP002345063-
OPPOSITION- STEINFELD R, ET AL, "A hypothesis on the biochemical mechanism of BH4-responsiveness in phenylalanine hydroxylase deficiency", AMINO ACIDS., SPRINGER VERLAG., AU, AU , (20030101), vol. 25, no. 1, ISSN 0939-4451, pages 63 - 68, XP002345063-
OPPOSITION- Tetrahydrobiopterin 10mg/50mg tablets, (20040107), XP055973919-
OPPOSITION- TREFZ F K, BLAU N, "POTENTIAL RATE OF TETRAHYDROBIOPTERIN IN THE TREATMENT OF MATERNAL PHENYLKETONURIA", Pediatrics, American Academy of Pediatrics, US, US , (20030101), vol. 112, no. 06 II, ISSN 0031-4005, pages 1566 - 1569, XP009053410-
OPPOSITION- M. Lindner, Haas, Mayatepek, Zschocke, Burgard, "Tetrahydrobiopterin Responsiveness in Phenylketonuria Differs between Patients with the Same Genotype", Molecular Genetics and Metabolism, Academic Press, (20010501), vol. 73, no. 1, doi:10.1006/mgme.2001.3168, ISSN 10967192, pages 104 - 106, XP055189088
OPPOSITION- Niederwieser A; Curtius H C; Wang M; Leupold D, "Atypical phenylketonuria with defective biopterin metabolism. Monotherapy with tetrahydrobiopterin or sepiapterin, screening and study of biosynthesis in", European Journal of Pediatrics, Springer Berlin Heidelberg, Berlin/Heidelberg, Berlin/Heidelberg, (19820301), vol. 138, no. 2, doi:10.1007/BF00441135, ISSN 0340-6199, pages 110 - 112, XP009168034
OPPOSITION- NIEDERWIESER A. et al., "Atypical Phenyketonuria with Defective Biopterin Metabolism. Monotherapy with Tethydrobiopterin or Sepiapterin, Screening und Study of Biosynthesis in Man", European Journal of Pediatrics, (19820000), XP009168034
OPPOSITION- TANAKA Y, ET AL., "ON-OFF PHENOMENON IN A CHILD WITH TETRAHYDROBIOPTERIN DEFICIENCY DUE TO 6-PYRUVOYL TETRAHYDROPTERIN SYNTHASE DEFICIENCY (BH4 DEFICIENCY)", European Journal of Pediatrics, Springer Berlin Heidelberg, Berlin/Heidelberg, Berlin/Heidelberg, (19890101), vol. 148, no. 05, doi:10.1007/BF00595911, ISSN 0340-6199, pages 450 - 452, XP008029347
OPPOSITION- NIEDERWIESER A; SHINTAKU H; LEIMBACHER W; CURTIUS H C; HYANEK J; ZEMAN J; ENDRES W, "PERIPHERAL TETRAHYDROBIOPTERIN DEFICIENCY WITH HYPERPHENYLALANINEMIA DUE TO INCOMPLETE 6 PYRUVOYLTETRAHYDROPTERIN SYNTHASE DEFICIENCY OR HETEROZYGOSITY", European Journal of Pediatrics, Springer Berlin Heidelberg, Berlin/Heidelberg, Berlin/Heidelberg, (19870101), vol. 146, no. 3, doi:10.1007/BF00716465, ISSN 0340-6199, pages 228 - 232, XP009168035
OPPOSITION- PONZONE A, ET AL., "DIFFERENTIAL DIAGNOSIS OF HYPERPHENYLALANINAEMIA BY A COMBINED PHENYLALANINE-TETRAHYDROBIOPTERIN LOADING TEST", European Journal of Pediatrics, Springer Berlin Heidelberg, Berlin/Heidelberg, Berlin/Heidelberg, (19930101), vol. 152, no. 08, doi:10.1007/BF01955242, ISSN 0340-6199, pages 655 - 661, XP009053425
OPPOSITION- PONZONE A, ET AL, "Differential diagnosis of hyperphenylalaninaemia by a combined phenylalanine-tetrahydrobiopterin loading test", European Journal of Pediatrics, Springer Berlin Heidelberg, Berlin/Heidelberg, Berlin/Heidelberg, (19930122), vol. 152, doi:10.1007/BF01955242, ISSN 0340-6199, pages 655 - 661, XP003032672
OPPOSITION- Steinfeld Robert; Kohlschütter Alfried; Zschocke Johannes; Lindner Martin; Ullrich Kurt; Lukacs Zoltan , "Tetrahydrobiopterin monotherapy for phenylketonuria patients with common mild mutations", European Journal of Pediatrics, Berlin/Heidelberg, (20020509), vol. 161, no. 7, doi:10.1007/s00431-002-0966-0, ISSN 0340-6199, pages 403 - 405, XP035493015
OPPOSITION- CERONE R,ET AL, "Long-term follow-up of a patient with mild tetrahydrobiopterin-responsive p henylketonuria", Molecular Genetics and Metabolism, Academic Press, AMSTERDAM, NL, AMSTERDAM, NL , (20040101), vol. 81, no. 2, doi:10.1016/j.ymgme.2003.11.008, ISSN 1096-7192, pages 137 - 139, XP002344606
OPPOSITION- Lücke Thomas, Illsinger Sabine, Aulehla-Scholz Christa, Sander Johannes, Das Anibh M., "BH4-sensitive hyperphenylalaninemia: New Case and Review of Literature", Pediatric Neurology, NL , (20030301), vol. 28, no. 3, doi:10.1016/S0887-8994(02)00516-7, ISSN 0887-8994, pages 228 - 230, XP055973521
OPPOSITION- BERNEGGER C et al., "HIGH FREQEUNCY OF TETRAHYDROBIOPTERIN- RESPONSIVENESS AMONG HYPERPHENYLALANINEMIAS:A STUDY OF 1919 PATIENTS OBSERVED FROM 1988 TO 2002", MOLECULAR GENETICS AND METABOLISM, AMSTERDAM, NL, (20020000), vol. 77, no. 4, ISSN 1096-7192, pages 304 - 313, XP008064071
OPPOSITION- Leo J.M Spaapen, M Estela Rubio-Gozalbo, "Tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency, state of the art", Molecular Genetics and Metabolism, Academic Press, AMSTERDAM, NL, AMSTERDAM, NL , (20030201), vol. 78, no. 2, doi:10.1016/S1096-7192(02)00229-9, ISSN 1096-7192, pages 93 - 99, XP055376651
OPPOSITION- Leo J.M Spaapen, M Estela Rubio-Gozalbo, "Tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency, state of the art", Molecular Genetics and Metabolism, AMSTERDAM, NL , (20030201), vol. 78, no. 2, doi:10.1016/S1096-7192(02)00229-9, ISSN 1096-7192, pages 93 - 99, XP055376651
OPPOSITION- Erlandsen H., Stevens R. C., "A structural hypothesis for BH4 responsiveness in patients with mild forms of hyperphenylalaninaemia and phenylketonuria", JOURNAL OF INHERITED METABOLIC DISEASE., KLUWER, DORDRECHT., NL, NL , (20010401), vol. 24, no. 2, doi:10.1023/A:1010371002631, ISSN 0141-8955, pages 213 - 230, XP055980076
OPPOSITION- L. J. M. Spaapen, Bakker J. A., Velter C., Loots W., Rubio-Gonzalbo M. E., Forget P. P., Dorland L., De Koning T. J., Poll-The B. T., Ploos Van Amstel H. K., Bekhof J., Blau N., Duran M., "Tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency in Dutch neonates.", JOURNAL OF INHERITED METABOLIC DISEASE., KLUWER, DORDRECHT., NL, NL , (20010101), vol. 24, no. 3, doi:10.1023/A:1010596317296, ISSN 0141-8955, pages 352 - 358, XP055376655
OPPOSITION- Ania C. Muntau, Wulf Röschinger, Matthias Habich, Hans Demmelmair, Björn Hoffmann, Christian P. Sommerhoff, Adelbert A. Roscher, "Tetrahydrobiopterin as an Alternative Treatment for Mild Phenylketonuria", New England Journal of Medicine, New England Journal of Medicine, (20021226), vol. 347, no. 26, doi:10.1056/NEJMoa021654, ISSN 00284793, pages 2122 - 2132, XP055189023
OPPOSITION- Sadao MATSUURA, Takashi SUGIMOTO, Shizuaki MURATA, Yoko SUGAWARA, Hitoshi IWASAKI, "Stereochemistry of Biopterin Cofactor and Facile Methods for the Determination of the Stereochemistry of a Biologically Active 5,6,7,8-Tetrahydropterin", Journal of Biochemistry, Oxford University Press, GB, GB , (19851101), vol. 98, no. 5, doi:10.1093/oxfordjournals.jbchem.a135401, ISSN 0021-924X, pages 1341 - 1348, XP009531512
OPPOSITION- Matalon Reuben, Koch Richard, Michals-Matalon Kimberlee, Moseley Kathryn, Surendran Sankar, Tyring Stephen, Erlandsen Heidi, Gamez Alejandra, Stevens Raymond C., Romstad Anne, Møller Lisbeth B., Guttler Flemming, "Biopterin responsive phenylalanine hydroxylase deficiency", Genetics in Medicine, Nature Publishing Group US, New York, New York, (20040101), vol. 6, no. 1, doi:10.1097/01.GIM.0000108840.17922.A7, ISSN 1098-3600, pages 27 - 32, XP055973528
OPPOSITION- Matalon Reuben, Koch Richard, Michals-Matalon Kimberlee, Moseley Kathryn, Surendran Sankar, Tyring Stephen, Erlandsen Heidi, Gamez Alejandra, Stevens Raymond C., Romstad Anne, Møller Lisbeth B., Guttler Flemming, "Biopterin responsive phenylalanine hydroxylase deficiency", Genetics in Medicine, New York, (20040101), vol. 6, no. 1, doi:10.1097/01.GIM.0000108840.17922.A7, ISSN 1098-3600, pages 27 - 32, XP055973528
OPPOSITION- Davis Michael D., Kaufman Seymour, Milstien Sheldon, "The auto-oxidation of tetrahydrobiopterin", European Journal of Biochemistry, Published by Springer-Verlag on behalf of the Federation of European Biochemical Societies, (19880401), vol. 173, no. 2, doi:10.1111/j.1432-1033.1988.tb14004.x, ISSN 0014-2956, pages 345 - 351, XP055860518
OPPOSITION- MATSUURA et al., "Highly stereoselective procedure for (6R)-tetrahydrobiopterin cofactor", Chemistry Letters, (19840000), doi:10.1246/cl.1984.735, pages 735 - 738, XP003028704
OPPOSITION- MATSUURA S, ET AL, "Highly stereoselective procedure for (6R)-tetrahydrobiopterin cofactor", Chemistry Letters, Chemical Society of Japan,Nippon Kagakukai, JP, JP , (19840101), doi:10.1246/cl.1984.735, ISSN 0366-7022, pages 735 - 738, XP003028704
SEARCH- Biomarin Pharmaceutical Inc, "KUVAN Consumer Medicine Information", (201201), Medsafe, URL: http://web.archive.org/web/20121014215930/http://www.medsafe.govt.nz/Consumers/cmi/k/kuvan.pdf, (20170116), XP002765924 [T] 1-13 * the whole document *-
SEARCH- Blau, "Disorders of tetrahydrobiopterin and related biogenic amines", (2001), URL: https://www.researchgate.net/profile/Beat_Thoeny/publication/233414667_Disorders_of_tetrahydrobiopterin_and_related_biogenic_amines/links/09e4150dddf878fbaf000000.pdf, (20170113), XP002765923 [A] 1-13 * the whole document *-
SEARCH- HENNERMANN J B ET AL, "Partial and total tetrahydrobiopterin-responsiveness in classical and mild phenylketonuria (PKU)", JOURNAL OF INHERITED METABOLIC DISEASE, KLUWER, DORDRECHT, NL, (20020906), vol. 25, no. Suppl.1, ISSN 0141-8955, page 21, XP009184263 [A] 1-13 * abstract *-
SEARCH- STEINFELD R ET AL, "A hypothesis on the biochemical mechanism of BH4-responsiveness in phenylalanine hydroxylase deficiency", AMINO ACIDS 2003 AUSTRIA, (200303), vol. 25, no. 1, ISSN 0939-4451, pages 63 - 68, XP002345063 [A] 1-13 * the whole document * * page 68, column 1 *-
SEARCH- TREFZ F K ET AL, "Potential Role of Tetrahydrobiopterin in the Treatment of Maternal Phenylketonuria", PEDIATRICS 2003 UNITED STATES, (2003), vol. 112, no. 6 II, ISSN 0031-4005, pages 1566 - 1569, XP009053410 [AP] 1-13 * abstract *-
SEARCH- M. LINDNER ET AL, "Tetrahydrobiopterin Responsiveness in Phenylketonuria Differs between Patients with the Same Genotype", MOLECULAR GENETICS AND METABOLISM, (200105), vol. 73, no. 1, doi:10.1006/mgme.2001.3168, ISSN 1096-7192, pages 104 - 106, XP055189088 [A] 1-13 * page 105 *
SEARCH- NIEDERWIESER A ET AL, "Atypical phenylketonuria with defective biopterin metabolism. Monotherapy with tetrahydrobiopterin or sepiapterin, screening and study of biosynthesis in", EUROPEAN JOURNAL OF PEDIATRICS, SPRINGER VERLAG, DE, (198203), vol. 138, no. 2, doi:10.1007/BF00441135, ISSN 0340-6199, pages 110 - 112, XP009168034 [A] 1-13 * page 110, column 2, paragraph last *
SEARCH- TANAKA Y ET AL, "ON-OFF PHENOMENON IN A CHILD WITH TETRAHYDROBIOPTERIN DEFICIENCY DUE TO 6-PYRUVOYL TETRAHYDROPTERIN SYNTHASE DEFICIENCY (BH4 DEFICIENCY)", EUROPEAN JOURNAL OF PEDIATRICS, SPRINGER VERLAG, DE, (1989), vol. 148, no. 5, doi:10.1007/BF00595911, ISSN 0340-6199, pages 450 - 452, XP008029347 [A] 1-13 * the whole document *
SEARCH- NIEDERWIESER A ET AL, "PERIPHERAL TETRAHYDROBIOPTERIN DEFICIENCY WITH HYPERPHENYLALANINEMIA DUE TO INCOMPLETE 6 PYRUVOYLTETRAHYDROPTERIN SYNTHASE DEFICIENCY OR HETEROZYGOSITY", EUROPEAN JOURNAL OF PEDIATRICS, SPRINGER VERLAG, DE, (1987), vol. 146, no. 3, doi:10.1007/BF00716465, ISSN 0340-6199, pages 228 - 232, XP009168035 [A] 1-13 * the whole document *
SEARCH- CERONE R ET AL, "Long-term follow-up of a patient with mild tetrahydrobiopterin-respo nsive phenylketonuria", MOLECULAR GENETICS AND METABOLISM 2004 UNITED STATES, (200402), vol. 81, no. 2, ISSN 1096-7192, pages 137 - 139, XP002344606 [AP] 1-13 * abstract *
SEARCH- BERNEGGER C ET AL, "HIGH FREQEUNCY OF TETRAHYDROBIOPTERIN-RESPONSIVENESS AMONG HYPERPHENYLALANINEMIAS:A STUDY OF 1919 PATIENTS OBSERVED FROM 1988 TO 2002", MOLECULAR GENETICS AND METABOLISM, ACADEMIC PRESS, AMSTERDAM, NL, (2002), vol. 77, no. 4, doi:10.1016/S1096-7192(02)00171-3, ISSN 1096-7192, pages 304 - 313, XP008064071 [A] 1-13 * page 311, column 1 *
SEARCH- ANIA C. MUNTAU ET AL, "Tetrahydrobiopterin as an Alternative Treatment for Mild Phenylketonuria", NEW ENGLAND JOURNAL OF MEDICINE, (20021226), vol. 347, no. 26, doi:10.1056/NEJMoa021654, ISSN 0028-4793, pages 2122 - 2132, XP055189023 [A] 1-13 * page 2127 *

Download Citation Report

Get a free citation report including examiner, opposition, and international search citations.

Get Citation Report

Dossier Documents

The dossier documents provide a comprehensive record of the patent’s prosecution history - including filings, correspondence, and decisions made by patent offices - and are crucial for understanding the patent’s legal journey and any challenges it may have faced during examination.

  • Date

    Description

  • Get instant alerts for new documents