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    1. Laurens, JB; Mbianda, XY; Ubbink, JB; Vermaak, WJH
      Gas chromatographic-mass spectrometric method for quantitation of phenylalanine and tyrosine in serum

      JOURNAL OF CHROMATOGRAPHY B
    2. Kuhara, T
      Diagnosis of inborn errors of metabolism using filter paper urine, urease treatment, isotope dilution and gas chromatography-mass spectrometry

      JOURNAL OF CHROMATOGRAPHY B
    3. Rashed, MS
      Clinical applications of tandem mass spectrometry: ten years of diagnosis and screening for inherited metabolic diseases

      JOURNAL OF CHROMATOGRAPHY B
    4. Yamaguchi, S; Iga, M; Kimura, M; Suzuki, Y; Shimozawa, N; Fukao, T; Kondo, N; Tazawa, Y; Orii, T
      Urinary organic acids in peroxisomal disorders: a simple screening method

      JOURNAL OF CHROMATOGRAPHY B
    5. Tzeng, CC; Lin, SJ; Chen, YJ; Kuo, PL; Jong, YJ; Tsai, LP; Chen, RM
      An effective strategy of using molecular testing to screen mentally retarded individuals for fragile X syndrome

      DIAGNOSTIC MOLECULAR PATHOLOGY
    6. Holzinger, A; Roschinger, W; Lagler, F; Mayerhofer, PU; Lichtner, P; Kattenfeld, T; Thuy, L; Nyhan, WL; Koch, HG; Muntau, AC; Roscher, AA
      Cloning of the human MCCA and MCCB genes and mutations therein reveal the molecular cause of 3-methylcrotonyl-CoA: carboxylase deficiency

      HUMAN MOLECULAR GENETICS
    7. Johnson, DW
      Analysis of amino acids as formamidene butyl esters by electrospray ionization tandem mass spectrometry

      RAPID COMMUNICATIONS IN MASS SPECTROMETRY
    8. Evengard, B; Petersson, K; Engman, ML; Wiklund, S; Ivarsson, SA; Tear-Fahnehjelm, K; Forsgren, M; Gilbert, R; Malm, G
      Low incidence of toxoplasma infection during pregnancy and in newborns in Sweden

      EPIDEMIOLOGY AND INFECTION
    9. Lucotte, G; Bathelier, C; Champenois, T
      PCR test for diagnosis of the common CJB2 (connexin 26) 35delG mutation ondried blood spots and determination of the carrier frequency in France

      MOLECULAR AND CELLULAR PROBES
    10. Weinhausel, A; Haas, OA
      Evaluation of the fragile X (FRAXA) syndrome with methylation-sensitive PCR

      HUMAN GENETICS
    11. Zschocke, J; Schulze, A; Lindner, M; Fiesel, S; Olgemoller, K; Hoffmann, GF; Penzien, J; Ruiter, JPN; Wanders, RJA; Mayatepek, E
      Molecular and functional characterisation of mild MCAD deficiency

      HUMAN GENETICS
    12. Sander, S; Janzen, N; Janetzky, B; Scholl, S; Steuerwald, U; Schafer, J; Sander, J
      Neonatal screening for medium chain acyl-CoA deficiency: high incidence inLower Saxony (northern Germany)

      EUROPEAN JOURNAL OF PEDIATRICS
    13. Braida, L; Crovella, S; Boniotto, M; Luchesi, A; de Vonderweid, U; Casetta, B; Amoroso, A
      A rapid and quantitative mass spectrometry method for determining the concentration of acylcarnitines and aminoacids in amniotic fluid

      PRENATAL DIAGNOSIS
    14. Love-Gregory, LD; Dyer, JA; Grasela, J; Hillman, RE; Phillips, CL
      Carrier detection and rapid newborn diagnostic test for the common Y393N maple syrup urine disease allele by PCR-RFLP: Culturally permissible testingin the Mennonite community

      JOURNAL OF INHERITED METABOLIC DISEASE
    15. Clayton, PT
      Applications of mass spectrometry in the study of inborn errors of metabolism

      JOURNAL OF INHERITED METABOLIC DISEASE
    16. Larsson, A
      Neonatal screening for metabolic, endocrine, infectious, and genetic disorders - Current and future directions

      CLINICS IN PERINATOLOGY
    17. Wood, JC; Magera, MJ; Rinaldo, P; Seashore, MR; Strauss, AW; Friedman, A
      Diagnosis of very long chain acyl-dehydrogenase deficiency from an infant's newborn screening card

      PEDIATRICS
    18. Hamvas, A; Trusgnich, M; Brice, H; Baumgartner, J; Hong, YL; Nogee, LM; Cole, FS
      Population-based screening for rare mutations: High-throughput DNA extraction and molecular amplification from Guthrie cards

      PEDIATRIC RESEARCH
    19. Meyburg, J; Schulze, A; Kohlmueller, D; Linderkamp, O; Mayatepek, E
      Postnatal changes in neonatal acylcarnitine profile

      PEDIATRIC RESEARCH
    20. Matern, D; Magera, MJ
      Mass spectrometry methods for metabolic and health assessment

      JOURNAL OF NUTRITION
    21. Craft, NE
      Innovative approaches to vitamin A assessment

      JOURNAL OF NUTRITION
    22. Mei, JV; Alexander, JR; Adam, BW; Hannon, WH
      Use of filter paper for the collection and analysis of human whole blood specimens

      JOURNAL OF NUTRITION
    23. Johnson, DW; ten Brink, HJ; Schuit, RC; Jakobs, C
      Rapid and quantitative analysis of unconjugated C-27 bile acids in plasma and blood samples by tandem mass spectrometry

      JOURNAL OF LIPID RESEARCH
    24. Shirtcliff, EA; Reavis, R; Overman, WH; Granger, DA
      Measurement of gonadal hormones in dried blood spots versus serum: Verification of menstrual cycle phase

      HORMONES AND BEHAVIOR
    25. Jensen, UG; Brandt, NJ; Christensen, E; Skovby, F; Norgaard-Pedersen, B; Simonsen, H
      Neonatal screening for galactosemia by quantitative analysis of hexose monophosphates using tandem mass spectrometry: A retrospective study

      CLINICAL CHEMISTRY
    26. Sweetman, L
      Newborn screening by tandem mass spectrometry: gaining experience

      CLINICAL CHEMISTRY
    27. Chamoles, NA; Blanco, M; Gaggioli, D
      Fabry disease: enzymatic diagnosis in dried blood spots on filter paper

      CLINICA CHIMICA ACTA
    28. Chace, DH
      Mass spectrometry in the clinical laboratory

      CHEMICAL REVIEWS
    29. Yoshioka, M; O'Neill, JP; Vacek, PM; Finette, BA
      Gestational age and gender-specific in utero V(D)J recombinase-mediated deletions

      CANCER RESEARCH
    30. Fasching, K; Panzer, S; Haas, OA; Borkhardt, A; Marschalek, R; Griesinger, F; Panzer-Grumayer, ER
      Presence of N regions in the clonotypic DJ rearrangements of the immunoglobulin heavy-chain genes indicates an exquisitely short latency in t(4;11)-positive infant acute lymphoblastic leukemia

      BLOOD
    31. Hardy, DT; Preece, MA; Green, A
      Determination of plasma free carnitine by electrospray tandem mass spectrometry

      ANNALS OF CLINICAL BIOCHEMISTRY
    32. Faradz, SMH; Leggo, J; Murray, A; Lam-Po-Tang, PRL; Buckley, MF; Holden, JJA
      Distribution of FMR1 and FMR2 alleles in Javanese individuals with developmental disability and confirmation of a specific AGG-interruption pattern in Asian populations

      ANNALS OF HUMAN GENETICS
    33. Andresen, BS; Dobrowolski, SF; O'Reilly, L; Muenzer, J; McCandless, SE; Frazier, DM; Udvari, S; Bross, P; Knudsen, I; Banas, R; Chace, DH; Engel, P; Naylor, EW; Gregersen, N
      Medium-chain Acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-Based prospective screening of newborns differ from those observed in patients with clinical symptoms: Identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency

      AMERICAN JOURNAL OF HUMAN GENETICS
    34. Elgstoen, KBP; Zhao, JY; Anacleto, JF; Jellum, E
      Potential of capillary electrophoresis, tandem mass spectrometry and coupled capillary electrophoresis-tandem mass spectrometry as diagnostic tools

      JOURNAL OF CHROMATOGRAPHY A
    35. Casetta, B; Tagliacozzi, D; Shushan, B; Federici, G
      Development of a method for rapid quantitation of amino acids by liquid chromatography-tandem mass spectrometry (LC-MSMS) in plasma

      CLINICAL CHEMISTRY AND LABORATORY MEDICINE
    36. Bonafe, L; Troxler, H; Kuster, T; Heizmann, CW; Chamoles, NA; Burlina, AB; Blau, N
      Evaluation of urinary acylglycines by electrospray tandem mass spectrometry in mitochondrial energy metabolism defects and organic acidurias

      MOLECULAR GENETICS AND METABOLISM
    37. Carnevale, S; Velasquez, JN; Labbe, JH; Chertcoff, A; Cabrera, MG; Rodriguez, MI
      Diagnosis of Enterocytozoon bieneusi by PCR in stool samples eluted from filter paper disks

      CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY
    38. Phillips, TM
      Assessing environmental exposure in children: immunotoxicology screening

      JOURNAL OF EXPOSURE ANALYSIS AND ENVIRONMENTAL EPIDEMIOLOGY
    39. Eastman, JW; Sherwin, JE; Wong, R; Liao, CL; Currier, RJ; Lorey, F; Cunningham, G
      Use of the phenylalanine : tyrosine ratio to test newborns for phenylketonuria in a large public health screening programme

      JOURNAL OF MEDICAL SCREENING
    40. Costa, CG; Guerand, WS; Struys, EA; Holwerda, U; ten Brink, HJ; de Almeida, IT; Duran, M; Jakobs, C
      Quantitative analysis of urinary acylglycines for the diagnosis of beta-oxidation defects using GC-NCI-MS

      JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS
    41. Fu, XW; Iga, M; Kimura, M; Yamaguchi, S
      Simplified screening for organic acidemia using GC/MS and dried urine filter paper: a study on neonatal mass screening

      EARLY HUMAN DEVELOPMENT
    42. Spielberg, F; Critchlow, C; Vittinghoff, E; Coletti, AS; Sheppard, H; Mayer, KH; Metzger, D; Judson, FN; Buchbinder, S; Chesney, M; Gross, M
      Home collection for frequent HIV testing: acceptability of oral fluids, dried blood spots and telephone results

      AIDS
    43. Qu, J; Wu, ZP; Luo, GA; Liu, MX; Yang, CD
      Newborn screening of phenylketonuria by LC/MS/MS

      CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE
    44. Beesley, R; Al Serouri, A; Filteau, SM
      Measurement of C-reactive protein in dried blood spots on filter paper

      TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE
    45. Tonniges, TF
      Serving the family from birth to the medical home - Newborn screening: A blueprint for the future - A call for a national agenda on state newborn screening programs

      PEDIATRICS
    46. Kirvar, E; Ilhan, T; Katzer, F; Hooshmand-Rad, P; Zweygarth, E; Gerstenberg, C; Phipps, P; Brown, CGD
      Detection of Theileria annulata in cattle and vector ticks by PCR using the Tams1 gene sequences

      PARASITOLOGY
    47. Sander, J; Janzen, N; Sander, S; Melchiors, U; Steuerwald, U
      Neonatal screening for inborn errors of metabolism using tandem mass spectrometry

      MONATSSCHRIFT KINDERHEILKUNDE
    48. Magera, MJ; Helgeson, JK; Matern, D; Rinaldo, P
      Methylmalonic acid measured in plasma and urine by stable-isotope dilutionand electrospray tandem mass spectrometry

      CLINICAL CHEMISTRY
    49. Yoon, HR; Paik, MJ; Shin, HS; Yu, C; Rinaldo, P
      Analysis of plasma free fatty acid cyanomethyl derivatives by GC-NPD for the diagnosis of mitochondrial fatty acid oxidation disorders

      CHROMATOGRAPHIA
    50. Craft, NE; Bulux, J; Valdez, C; Li, YK; Solomons, NW
      Retinol concentrations in capillary dried blood spots from healthy volunteers: method validation

      AMERICAN JOURNAL OF CLINICAL NUTRITION
    51. Shigematsu, Y; Hata, I; Kikawa, Y; Mayumi, M; Tanaka, Y; Sudo, M; Kado, N
      Modifications in electrospray tandem mass spectrometry for a neonatal-screening pilot study in Japan

      JOURNAL OF CHROMATOGRAPHY B
    52. Kuhara, T; Shinka, T; Inoue, Y; Ohse, M; Xia, ZW; Yoshida, I; Inokuchi, T; Yamaguchi, S; Takayanagi, M; Matsumoto, I
      Pilot study of gas chromatographic-mass spectrometric screening of newbornurine for inborn errors of metabolism after treatment with urease

      JOURNAL OF CHROMATOGRAPHY B
    53. McCarron, B; Fox, R; Wilson, K; Cameron, S; McMenamin, J; McGregor, G; Pithie, A; Goldberg, D
      Hepatitis C antibody detection in dried blood spots

      JOURNAL OF VIRAL HEPATITIS
    54. Chace, DH; Naylor, EW
      Expansion of newborn screening programs using automated tandem mass spectrometry

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    55. Mushtaq, I; Logan, S; Morris, M; Johnson, AW; Wade, AM; Kelly, D; Clayton, PT
      Screening of newborn infants for cholestatic hepatobiliary disease with tandem mass spectrometry

      BRITISH MEDICAL JOURNAL
    56. Johnson, DW
      Dimethylaminoethyl esters for trace, rapid analysis of fatty acids by electrospray tandem mass spectrometry

      RAPID COMMUNICATIONS IN MASS SPECTROMETRY
    57. Naylor, EW; Chace, DH
      Automated tandem mass spectrometry for mass newborn screening for disorders in fatty acid, organic acid, and amino acid metabolism

      JOURNAL OF CHILD NEUROLOGY
    58. Pollitt, RJ
      Tandem mass spectrometry screening: proving effectiveness

      ACTA PAEDIATRICA
    59. Chace, DH; DiPerna, JC; Naylor, EW
      Laboratory integration and utilization of tandem mass spectrometry in neonatal screening: a model for clinical mass spectrometry in the next millennium

      ACTA PAEDIATRICA
    60. Wiley, V; Carpenter, K; Wilcken, B
      Newborn screening with tandem mass spectrometry: 12 months' experience in NSW Australia

      ACTA PAEDIATRICA
    61. Dobrowolski, SF; Banas, RA; Naylor, EW; Powdrill, T; Thakkar, D
      DNA microarray technology for neonatal screening

      ACTA PAEDIATRICA
    62. Norgaard-Pedersen, B; Simonsen, H
      Biological specimen banks in neonatal screening

      ACTA PAEDIATRICA
    63. Beeso, J; Wong, N; Ayling, R; Eldridge, P; Marshall, W; Sherwood, R; Peters, T
      Screening for hypercholesterolaemia in 10,000 neonates in a multi-ethnic population

      EUROPEAN JOURNAL OF PEDIATRICS
    64. Rashed, MS; Rahbeeni, Z; Ozand, PT
      Application of electrospray tandem mass spectrometry to neonatal screening

      SEMINARS IN PERINATOLOGY
    65. Rinaldo, P; Yoon, HR; Yu, CL; Raymond, K; Tiozzo, C; Giordano, G
      Sudden and unexpected neonatal death: A protocol for the postmortem diagnosis of fatty acid oxidation disorders

      SEMINARS IN PERINATOLOGY
    66. Bartlett, K; Pourfarzam, M
      Tandem mass spectrometry - The potential

      JOURNAL OF INHERITED METABOLIC DISEASE
    67. Green, A; Pollitt, RJ
      Population newborn screening for inherited metabolic disease: Current UK perspectives

      JOURNAL OF INHERITED METABOLIC DISEASE
    68. Al Aqeel, AI; Rashed, MS; Wanders, RJA
      Carnitine-acylcarnitine translocase deficiency is a treatable disease

      JOURNAL OF INHERITED METABOLIC DISEASE
    69. Vreken, P; van Lint, AEM; Bootsma, AH; Overmars, H; Wanders, RJA; van Gennip, AH
      Quantitative plasma acylcarnitine analysis using electrospray tandem mass spectrometry for the diagnosis of organic acidaemias and fatty acid oxidation defects

      JOURNAL OF INHERITED METABOLIC DISEASE
    70. Wiemels, JL; Cazzaniga, G; Daniotti, M; Eden, OB; Addison, GM; Masera, G; Saha, V; Biondi, A; Greaves, MF
      Prenatal origin of acute lymphoblastic leukaemia in children

      LANCET
    71. Sander, J; Janzen, N
      Optimized laboratory technics for neonatal screening for phenylketonuria and other hyperphenylalaninemias

      MONATSSCHRIFT KINDERHEILKUNDE
    72. Poplawski, NK; Ranieri, E; Harrison, JR; Fletcher, JM
      Multiple acyl-coenzyme A dehydrogenase deficiency: Diagnosis by acyl-carntine analysis of a 12-year-old newborn screening card

      JOURNAL OF PEDIATRICS
    73. Russeva, MG; Janakiev, PJ; Kirov, SA; Paskaleva, ID; Kremensky, IM; Penner, JA; Hassouna, HS; Ganev, VS
      A simple method for detection of factor V R506Q (Leiden) mutation in driedblood spots

      CLINICA CHIMICA ACTA
    74. Heath, EM; O'Brien, DP; Banas, R; Naylor, EW; Dobrowolski, S
      Optimization of an automated DNA purification protocol for neonatal screening

      ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE
    75. Linder, N; Davidovitch, N; Kogan, A; Barzilai, A; Kuint, J; Mazkeret, R; Sack, J
      Longitudinal measurements of 17 alpha-hydroxyprogesterone in premature infants during the first three months of life

      ARCHIVES OF DISEASE IN CHILDHOOD
    76. Andresen, BS; Olpin, S; Poorthuis, BJHM; Scholte, HR; Vianey-Saban, C; Wanders, R; Ijlst, L; Morris, A; Pourfarzam, M; Bartlett, K; Baumgartner, ER; deKlerk, JBC; Schroeder, LD; Corydon, TJ; Lund, H; Winter, V; Bross, P; Bolund, L; Gregersen, N
      Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiency

      AMERICAN JOURNAL OF HUMAN GENETICS
    77. LIPPI G; GUIDI G
      STANDARDIZATION AND CLINICAL MANAGEMENT OF LIPOPROTEIN(A) MEASUREMENTS

      CLINICAL CHEMISTRY AND LABORATORY MEDICINE
    78. CAGGANA M; CONROY JM; PASS KA
      RAPID, EFFICIENT METHOD FOR MULTIPLEX AMPLIFICATION FROM FILTER-PAPER

      Human mutation
    79. THOMASON MJ; LORD J; BAIN MD; CHALMERS RA; LITTLEJOHNS P; ADDISON GM; WILCOX AH; SEYMOUR CA
      A SYSTEMATIC REVIEW OF EVIDENCE FOR THE APPROPRIATENESS OF NEONATAL SCREENING PROGRAMS FOR INBORN-ERRORS OF METABOLISM

      Journal of public health medicine
    80. ALESSA M; BAKHEET S; PATAY Z; ALWATBAN J; POWE J; JOSHI S; OZAND PT
      (18)FLUORO-2-DEOXYGLUCOSE ((18)FDG) PET SCAN OF THE BRAIN IN GLUTARICACIDURIA TYPE-1 - CLINICAL AND MRI CORRELATIONS

      Brain & development
    81. NELSON KB; DAMBROSIA JM; GRETHER JK; PHILLIPS TM
      NEONATAL CYTOKINES AND COAGULATION-FACTORS IN CHILDREN WITH CEREBRAL-PALSY

      Annals of neurology
    82. PATEL VC; MCCLENDON RW; GOODRUM JW
      COLOR COMPUTER VISION AND ARTIFICIAL NEURAL NETWORKS FOR THE DETECTION OF DEFECTS IN POULTRY EGGS

      Artificial intelligence review
    83. ALESSA M; RASHED M; OZAND PT
      SAUDI EXPERIENCE WITH CLASSIC HOMOCYSTINURIA

      Annals of saudi medicine
    84. OZAND PT
      DIAGNOSIS OF INBORN-ERRORS OF METABOLISM BY TANDEM MASS-SPECTROMETRY

      Annals of saudi medicine
    85. ALTINDAG ZZ; SAHIN G; INANICI F; HASCELIK Z
      URINARY NEOPTERIN EXCRETION AND DIHYDROPTERIDINE REDUCTASE-ACTIVITY IN RHEUMATOID-ARTHRITIS

      Rheumatology international
    86. MAKOWSKI GS; HOPFER SM
      CYSTIC-FIBROSIS - MOLECULAR APPROACHES TO DIAGNOSIS

      Annals of clinical and laboratory science
    87. MAKOWSKI GS; DAVIS EL; NADEAU F; HOPFER SM
      POLYMERASE-CHAIN-REACTION AMPLIFICATION OF GUTHRIE CARD DEOXYRIBONUCLEIC-ACID - EXTRACTION OF NUCLEIC-ACID FROM FILTER MATRICES

      Annals of clinical and laboratory science
    88. PARRA MJA; MATEOS AA; MATA MM; DEMARIA CG
      ENZYMATIC FLOW-INJECTION DETERMINATION OF L-PHENYLALANINE USING THE STOPPED-FLOW AND MERGING-ZONES TECHNIQUES

      Talanta
    89. COATES GL; GUARENTI L; PARKER SP; WILLUMSEN JF; TOMKINS AM
      EVALUATION OF THE SENSITIVITY AND SPECIFICITY OF A TREPONEMA-PALLIDUMDRIED BLOOD SPOT TECHNIQUE FOR USE IN THE DETECTION OF SYPHILIS

      Transactions of the Royal Society of Tropical Medicine and Hygiene
    90. WAY LJ; HUBBARD RW
      DETERMINATION OF FREE AND TOTAL CARNITINE WITH A RANDOM-ACCESS CHEMISTRY ANALYZER

      Clinical chemistry
    91. Levy, HL
      Newborn screening by tandem mass spectrometry: A new era

      CLINICAL CHEMISTRY
    92. Chace, DH; Sherwin, JE; Hillman, SL; Lorey, F; Cunningham, GC
      Use of phenylalanine-to-tyrosine ratio determined by tandem mass spectrometry to improve newborn screening for phenylketonuria of early discharge specimens collected in the first 24 hours

      CLINICAL CHEMISTRY
    93. CLAYTON PT; DOIG M; GHAFARI S; MEANEY C; TAYLOR C; LEONARD JV; MORRIS M; JOHNSON AW
      SCREENING FOR MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY USING ELECTROSPRAY-IONIZATION TANDEM MASS-SPECTROMETRY

      Archives of Disease in Childhood
    94. TAWA R; MATSUNAGA H; FUJIMOTO T
      HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC ANALYSIS OF AMINOGLYCOSIDE ANTIBIOTICS

      Journal of chromatography
    95. LI XL; DEHOFFMAN E
      ION CHEMISTRY OF DEPROTONATED PHENYLTHIOCARBAMYL-PHENYLALANINE

      Journal of the American Society for Mass Spectrometry
    96. ANDRESEN BS; BROSS P; UDVARI S; KIRK J; GRAY G; KMOCH S; CHAMOLES N; KNUDSEN I; WINTER V; WILCKEN B; YOKOTA I; HART K; PACKMAN S; HARPEY JP; SAUDUBRAY JM; HALE DE; BOLUND L; KOLVRAA S; GREGERSEN N
      THE MOLECULAR-BASIS OF MEDIUM-CHAIN ACYL-COA DEHYDROGENASE (MCAD) DEFICIENCY IN COMPOUND HETEROZYGOUS PATIENTS - IS THERE CORRELATION BETWEEN GENOTYPE AND PHENOTYPE

      Human molecular genetics
    97. PARKER SP; CUBITT WD; ADES AE
      A METHOD FOR THE DETECTION AND CONFIRMATION OF ANTIBODIES TO HEPATITIS-C VIRUS IN DRIED BLOOD SPOTS

      Journal of virological methods
    98. LOFFREDO CA; EWING CK
      USE OF STORED NEWBORN BLOOD SPOTS IN RESEARCH ON BIRTH-DEFECTS - VARIATION IN RETRIEVAL RATES BY TYPE OF DEFECT AND INFANT CHARACTERISTICS

      American journal of medical genetics
    99. CASSOL S; GILL MJ; PILON R; CORMIER M; VOIGT RF; WILLOUGHBY B; FORBES J
      QUANTIFICATION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 RNA FROM DRIED PLASMA SPOTS COLLECTED ON FILTER-PAPER

      Journal of clinical microbiology
    100. ELNAGAR B; GEBREMEDHIN M; LARSSON A; KARLSSON FA
      IODINE NUTRITION IN SUDAN - DETERMINATION OF THYROID-STIMULATING HORMONE IN FILTER-PAPER BLOOD-SAMPLES

      Scandinavian journal of clinical & laboratory investigation


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Documento generato il 01/06/20 alle ore 08:19:02