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: 6875715)

  • 1. Multiple ankyloses, facial anomalies, and pulmonary hypoplasia associated with severe antenatal spinal muscular atrophy.
    Moerman P; Fryns JP; Goddeeris P; Lauweryns JM
    J Pediatr; 1983 Aug; 103(2):238-41. PubMed ID: 6875715
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Arthrogryposis accompanying congenital spinal-type muscular atrophy.
    Besser M; Behar A
    Arch Dis Child; 1967 Dec; 42(226):666-70. PubMed ID: 6073835
    [No Abstract]   [Full Text] [Related]  

  • 3. The syndrome of multiple ankyloses and facial anomalies. A neuropathologic analysis.
    Williams RS; Holmes LB
    Acta Neuropathol; 1980; 50(3):175-9. PubMed ID: 7415811
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Syndrome of ankylosis, facial anomalies, and pulmonary hypoplasia.
    Punnett HH; Kistenmacher ML; Valdes-Dapena M; Ellison RT
    J Pediatr; 1974 Sep; 85(3):375-7. PubMed ID: 4154411
    [No Abstract]   [Full Text] [Related]  

  • 5. Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia: a lethal condition.
    Pena SD; Shokeir MH
    J Pediatr; 1974 Sep; 85(3):373-5. PubMed ID: 4431498
    [No Abstract]   [Full Text] [Related]  

  • 6. Neuropathologic findings in the spinal cords of 10 infants with arthrogryposis.
    Clarren SK; Hall JG
    J Neurol Sci; 1983 Jan; 58(1):89-102. PubMed ID: 6842261
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pulmonary hypoplasia, multiple ankyloses, and camptodactyly: one syndrome or some related forms?
    Lazjuk GI; Cherstvoy ED; Lurie IW; Nedzved MK
    Helv Paediatr Acta; 1978 Apr; 33(1):73-9. PubMed ID: 669973
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Syndrome of camptodactyly, ankyloses, facial anomalies, and pulmonary hypoplasia (Pena-Shokeir syndrome): obstetric and ultrasound aspects.
    Shenker L; Reed K; Anderson C; Hauck L; Spark R
    Am J Obstet Gynecol; 1985 Jun; 152(3):303-7. PubMed ID: 3890548
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Syndrome of ankylosis, facial anomalies, and pulmonary hypoplasia: a pathologic analysis of one infant.
    Dimmick JE; Berry K; MacLeod PM; Hardwick DF
    Birth Defects Orig Artic Ser; 1977; 13(3D):133-7. PubMed ID: 922132
    [No Abstract]   [Full Text] [Related]  

  • 10. Spinal muscular atrophy syndromes.
    Low NL
    Pediatr Ann; 1977 Mar; 6(3):162-8. PubMed ID: 846758
    [No Abstract]   [Full Text] [Related]  

  • 11. Arthrogryposis multiplex congenita, Pena-Shokeir phenotype, with gastroschisis and agenesis of the leg.
    Agapitos M; Georgiou-Theodoropoulou M; Koutselinis A; Papacharalambus N
    Pediatr Pathol; 1988; 8(4):409-13. PubMed ID: 2974953
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Two cases of fetal akinesia/hypokinesia sequence.
    Itoh K; Yokoyama N; Ishihara A; Kawai S; Takada S; Nishino M; Lee Y; Negishi H; Itoh H
    Pediatr Pathol; 1991; 11(3):467-77. PubMed ID: 1866365
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Syndrome of camptodactyly, multiple ankyloses, facial anomalies and pulmonary hypoplasia--further delineation and evidence for autosomal recessive inheritance.
    Pena SD; Shokeir MH
    Birth Defects Orig Artic Ser; 1976; 12(5):201-8. PubMed ID: 953225
    [No Abstract]   [Full Text] [Related]  

  • 14. Arthrogryposis multiplex congenita: an autopsy case of a fatal form.
    Imamura M; Yamanaka N; Nakamura F; Oyanagi K
    Hum Pathol; 1981 Aug; 12(8):699-704. PubMed ID: 7286967
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Familial akinesia-hypokinesia sequence (Pena-Shokier phenotype)].
    Oberlechner E; Seidel H; Schramm T; Rehder H; Gullotta F; Stechele F; Högel B; Rothemund E; Fichtel G
    Geburtshilfe Frauenheilkd; 1994 May; 54(5):276-85. PubMed ID: 8050688
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A syndrome of ankylosis, facial anomalies and pulmonary hypoplasia secondary to fetal neuromuscular dysfunction.
    Mease AD; Yeatman GW; Pettett G; Merenstein GB
    Birth Defects Orig Artic Ser; 1976; 12(5):193-200. PubMed ID: 953224
    [No Abstract]   [Full Text] [Related]  

  • 17. Olivo-ponto-cerebellar atrophy with muscular atrophy, joint contractures and pulmonary hypoplasia of prenatal onset.
    Moerman P; Barth PG
    Virchows Arch A Pathol Anat Histopathol; 1987; 410(4):339-45. PubMed ID: 3101283
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Arthrogryposis multiplex congenita: spectrum of pathologic changes.
    Banker BQ
    Hum Pathol; 1986 Jul; 17(7):656-72. PubMed ID: 3721492
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Clinical and ultrastructural study of a case of arthrogryposis].
    Martin C; Vital C; Babin JP; Vallat JM; Heheunstre JP
    Arch Fr Pediatr; 1971 Apr; 28(4):445-6. PubMed ID: 5087589
    [No Abstract]   [Full Text] [Related]  

  • 20. [Features of progressive muscular dystrophy, infantile spinal muscular atrophy, and congenital multiple arthrogryposis].
    Erak P; Zeskov P; Vukadinović S; Kalafatić Z
    Neurologija; 1978; 26(1-4):223-9. PubMed ID: 754026
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.