Neonatal diagnosis of hereditary metabolic diseases
Lambotte, C.
Revue Medicale de Liege 28(24): 837-851
1973
ISSN/ISBN: 0370-629X PMID: 4769974 Document Number: 68243
Document emailed within 1 workday
Related Documents
Moser, H. 1983: Prenatal diagnosis of metabolic diseases and monogenic hereditary diseases Gynakologische Rundschau 22(Suppl 3): 33-47Sviatkina, O.B. 1971: Laboratory diagnosis of hereditary metabolic diseases Meditsinskaia Sestra 30(8): 16-18
Divry, P.; Maire, I.; Mathieu, M. 1988: Biological diagnosis of hereditary metabolic diseases. from selective screening to the mutant-cell bank Annales de Biologie Clinique 46(6): 381-386
Barashnev, I.I.; Kozlova, S.I. 1971: Early diagnosis of hereditary metabolic disorders as an effective means of preventing nervous system diseases in children Zhurnal Nevropatologii i Psikhiatrii Imeni S.S. Korsakova 71(10): 1470-1474
Skovby, F. 1998: Neonatal screening for hereditary diseases Ugeskrift for Laeger 160(40): 5765
Hultberg, B.; Sjöblad, S.; Ockerman, P.A. 1974: Hereditary metabolic diseases with cumulative symptoms Lakartidningen 71(26): 2631-2637
Vidailhet, M. 1991: Recent progress in hereditary metabolic diseases Archives Francaises de Pediatrie 48(8): 581-584
Tkachev, R.A.; Markova, E.D.; Gotovtseva, E.V.; Bauman, L.K.; Barkhatova, V.P. 1970: The pathogenetic significance of metabolic disorders in hereditary extrapyramial diseases Zhurnal Nevropatologii i Psikhiatrii Imeni S.S. Korsakova 70(4): 512-520
Kaabachi, N.; Mebazaa, A.; Hamza, L.; Ben Miled, S.; Abdelmoula, J. 1989: Organized detection of hereditary metabolic diseases. Amino acidopathies and organic acidurias La Tunisie Medicale 67(11): 697-701
Kok, A.J.; van Zoeren-Grobben, D.; van de Bor, M.; Mooy, P.D.; van Gelderen, H.H. 1985: Diagnosis of hereditary metabolic disorders in newborn and young infants Tijdschrift Voor Kindergeneeskunde 53(1): 1-7
Lanza, I. 1975: Multiple screening tests for hereditary metabolic diseases. Clinical problems and questions of interpretation Minerva Pediatrica 27(37): 2054-2064
Oscarson, M.; Vassiliou, D.; Nordenström, A.; Nergårdh, R.; Wedell, A.; von Döbeln, U. 2016: Hereditary metabolic diseases with onset in adulthood. Early and correct treatment of acute symptoms can be life-saving Lakartidningen 113
Sasaki, H. 1990: DNA diagnosis of hereditary diseases Nihon Rinsho. Japanese Journal of Clinical Medicine 48 Suppl: 1073-1077
Ars, E.; Torra, R.; Oliver, A. 2003: Molecular diagnosis of hereditary renal diseases Nefrologia: Publicacion Oficial de la Sociedad Espanola Nefrologia 23(Suppl 1): 2-10
Kosovský, J.; Turna, J. 1989: Use of recombinant DNA technics in the diagnosis of hereditary diseases Bratislavske Lekarske Listy 90(7): 532-539
Ginter, E.K.; Budagova, K.A.; Revazov, A.A.; Petrin, A.N.; Bugaeva, E.A. 1986: Medico-genetical study of the Uzbekistan population. IX. Variability of hereditary pathology, territorial distribution of hereditary diseases and hereditary disease load in the population of the Urgut district of the Samarkand region Genetika 22(7): 1199-1206
Rumenić-Garzicić, L.; Krajinović, M. 1985: Prenatal diagnosis of hereditary diseases using chorionic villi Jugoslavenska Ginekologija i Perinatologija 25(1-2): 25-28
Baranov, V.S.; Vakharlovskiĭ, V.G.; Aĭlamazian, E.K. 1994: Prenatal diagnosis and prevention of congenital and hereditary diseases Akusherstvo i Ginekologiia 1994(6): 8-11
Steuer, W. 1971: Early diagnosis of congenital metabolic diseases Minerva Medica 62(83): 4047-4052
Taguchi, T. 2007: Antenatal diagnosis of neonatal surgical diseases Nihon Geka Gakkai Zasshi 108(6): 318-324