These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

112 related articles for article (PubMed ID: 4213902)

  • 1. [Sanfilippo's disease: clinico-genetic and biological study of 2 families].
    Carlomagno S; Federico A; Vitiello F; Pinto L; Vertucci P; Marolda M; Balbi R; Guazzi GC
    Acta Neurol (Napoli); 1974; 29(3):231-51. PubMed ID: 4213902
    [No Abstract]   [Full Text] [Related]  

  • 2. [A comparative clinical, radiologic, biochemical and genetic study of Sanfilippo's disease, type A and B. Six case reports].
    Farriaux JP; Dhondt JL; Blanckaert D; Fontaine G
    Helv Paediatr Acta; 1974 Oct; 29(4):349-70. PubMed ID: 4214802
    [No Abstract]   [Full Text] [Related]  

  • 3. [Mucopolysaccharidosis III (Sanfilippo's syndrome): phenotypic characterization].
    Mendes FT; Ciorlia VR; Lamego C; de Almeida SP; de Ulhoa-Cintra AB
    Rev Hosp Clin Fac Med Sao Paulo; 1976; 31(6):478-83. PubMed ID: 827800
    [No Abstract]   [Full Text] [Related]  

  • 4. [1st Italian family affected by type A Sanfilippo's disease].
    Carlomagno S; Militerni R; Pascotto A; Guazzi GC
    Acta Neurol (Napoli); 1977; 32(1):97-107. PubMed ID: 404848
    [No Abstract]   [Full Text] [Related]  

  • 5. [Sanfilippo's disease of type B. Study of the enzymatic deficiency in a family].
    Nobili B; Iolascon A; Bello L; Chianese C; Rasulo V; Iolascon G; Pinto L
    Pediatria (Napoli); 1983; 91(2-3):295-301. PubMed ID: 6420769
    [No Abstract]   [Full Text] [Related]  

  • 6. [Clinical, radiological, biochemical, and genetic aspects of the Sanfilippo disease, apropos of 3 cases].
    Dhondt JL; Farriaux JP; Fournier A; Fontaine G
    J Genet Hum; 1974 Jun; 22(2):109-32. PubMed ID: 4278846
    [No Abstract]   [Full Text] [Related]  

  • 7. Report of three cases of mucopolysacchaidoses and an unusual case of hyperaminoaciduria detected during the screening of mentally retarded children.
    Devi KS; Veeraju P; Rao BS
    Hum Hered; 1994; 44(2):90-3. PubMed ID: 8188315
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Spondyloepiphyseal dysplasia.
    Spranger J; Langer LO
    Birth Defects Orig Artic Ser; 1974; 10(9):19-61. PubMed ID: 4213775
    [No Abstract]   [Full Text] [Related]  

  • 9. Sanfilippo's syndrome type C--the first known case in South Africa.
    Petersen EM
    S Afr Med J; 1986 Jan; 69(1):63-8. PubMed ID: 3079922
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Chronic plumbism in siblings with Sanfilippo's mucopolysaccharidosis].
    Hager-Malecka B; Sroczyńska M; Sychlowy A; Sońta-Jakimczyk D; Dziuba P; Król J
    Pediatr Pol; 1977 Jun; 52(6):659-63. PubMed ID: 406592
    [No Abstract]   [Full Text] [Related]  

  • 11. Morphological and biochemical findings in a case of mucopolysaccharidosis type III A (Sanfilippo's disease type A).
    Witting C; Müller KM; Kresse H; Figura KV; Marx H
    Beitr Pathol; 1975; 154(3):324-38. PubMed ID: 805586
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The Dyggve-Melchior-Clausen syndrome.
    Spranger J; Maroteaux P; Der Kaloustian VM
    Radiology; 1975 Feb; 114(2):415-21. PubMed ID: 803318
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Sanfilippo's syndrome].
    Orii T
    Nihon Rinsho; 1977; 35 Suppl 1():1068-9. PubMed ID: 418202
    [No Abstract]   [Full Text] [Related]  

  • 14. [2 further cases of Dyggve-Melchior-Clausen syndrome with hypoplasia of the odontoid apophysis and spinal compression].
    Naffah J; Taleb N
    Arch Fr Pediatr; 1974 Dec; 31(10):985-92. PubMed ID: 4219130
    [No Abstract]   [Full Text] [Related]  

  • 15. [Characteristics of urinary heparan sulfate in 5 cases of Sanfilippo's syndrome].
    Fossati G; Sinigaglia F; Calatroni A
    Boll Soc Ital Biol Sper; 1974 Oct; 50(19):1552-8. PubMed ID: 4282024
    [No Abstract]   [Full Text] [Related]  

  • 16. [Sanfilippo's syndrome: typing of mucopolisaccharides in urine and enzymatic determination in plasma].
    Burrows R; Muzzo S
    Rev Chil Pediatr; 1980; 51(2):129-33. PubMed ID: 6448458
    [No Abstract]   [Full Text] [Related]  

  • 17. [Visual diagnosis: diastrophic dwarfism (Lamy-Maroteaux syndrome)].
    Gerhardt R; Stichel W
    Beitr Orthop Traumatol; 1989 Dec; 36(12):575-80. PubMed ID: 2514681
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A new dominant gene mental retardation syndrome. Association with small stature, tapering fingers, characteristic facies, and possible hydrocephalus.
    Lowry B; Miller JR; Fraser FC
    Am J Dis Child; 1971 Jun; 121(6):496-500. PubMed ID: 5581017
    [No Abstract]   [Full Text] [Related]  

  • 19. [A dominant syndrome associated with polysyndactyly, spatule thumb, facial abnormalities, and mental retardation. (A particular form of Noack's acrocephalosyndactylia)].
    Gnamey D; Farriaux JP
    J Genet Hum; 1971 Dec; 19(4):299-316. PubMed ID: 5152131
    [No Abstract]   [Full Text] [Related]  

  • 20. Dyggve-Melchior-Clausen syndrome: genetic studies and report of affected sibs.
    Toledo SP; Saldanha PH; Lamego C; Mourão PA; Dietrich CP; Mattar E
    Am J Med Genet; 1979; 4(3):255-61. PubMed ID: 117710
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.