129 related articles for article (PubMed ID: 5058493)
1. [Fatal congenital hypophosphatasia].
Péter J; Ferenczy I; Görgényi A; Machay T
Orv Hetil; 1972 Jan; 113(5):258-60. PubMed ID: 5058493
[No Abstract] [Full Text] [Related]
2. [Study of congenital osteodystrophies. Considerations on 4 cases of Rathbun's hypophosphatasia and 7 unusual cases of rachitic osteodystrophy].
Tirnoveanu G; Georgescu MI; Mitescu G
Rev Med Chir Soc Med Nat Iasi; 1972; 16(3):667-72. PubMed ID: 5080559
[No Abstract] [Full Text] [Related]
3. Familial hyperphosphatasemia with ateliosis and hypermetabolism of growing membranous bone; review of the clinical, radiographic and chemical features.
Caffey J
Bull Hosp Joint Dis; 1972 Oct; 33(2):81-110. PubMed ID: 4648260
[No Abstract] [Full Text] [Related]
4. Isoenzymes of alkaline phosphatase in infantile hypophosphatasia.
Mueller HD; Stinson RA; Mohyuddin F; Milne JK
J Lab Clin Med; 1983 Jul; 102(1):24-30. PubMed ID: 6854132
[TBL] [Abstract][Full Text] [Related]
5. Pedigree of a family with hyper-alkaline-phosphatasemia apparently inherited as an autosomal recessive trait.
Kawasaki S; Sano M; Nagumo F; Tadano J; Maeda T
Clin Chim Acta; 1995 Jun; 238(1):109-11. PubMed ID: 7554291
[No Abstract] [Full Text] [Related]
6. [Hypophosphatasia].
Beck C; Morbach H; Stenzel M; Schneider P; Collmann H; Girschick G; Girschick HJ
Klin Padiatr; 2009; 221(4):219-26. PubMed ID: 19629901
[TBL] [Abstract][Full Text] [Related]
7. Estimation of the frequency of the recessive gene of acatalasemia in Japan.
Ogata M; Hayashi S; Takahara S
Acta Med Okayama (1952); 1971 Jun; 25(3):193-8. PubMed ID: 4263520
[No Abstract] [Full Text] [Related]
8. Autosomal recessive adult-onset hypophosphatasia.
Harraway JR; Sheard JM; Soule SJ; Florkowski CM; George PM
Pathology; 2005 Dec; 37(6):563-5. PubMed ID: 16373239
[No Abstract] [Full Text] [Related]
9. Congenital hypophosphatasia. Report on two cases with special reference to phosphoethanolamine excretion.
Terheggen HG; Schildberg C; Schürer W; Van Sande M; Bützler O
Monogr Hum Genet; 1972; 6():188. PubMed ID: 4663897
[No Abstract] [Full Text] [Related]
10. [Neonatal discovery of hypophosphatasia. Bone improvement. Fatal convulsant encephalopathy].
Béthenod M; Cotte MF; Collombel C; Fréderich A; Cotte J
Ann Pediatr (Paris); 1967 Dec; 14(12):835-41. PubMed ID: 4299440
[No Abstract] [Full Text] [Related]
11. [Morphological and clinical contribution to lethal congenital hypophosphatasia].
Justus J; Rupprecht E; Recknagel R; Justus B
Kinderarztl Prax; 1974 Apr; 42(4):148-55. PubMed ID: 4473022
[No Abstract] [Full Text] [Related]
12. [Idiopathic transient hyperphosphatemia in an infant. Apropos of 2 observations].
Gairi Tahull JM; Camarasa Piquer F; Caritg Bosch J; Castellanos Bermúdez S; Herrero Gimeno J
An Esp Pediatr; 1983 Jun; 18(6):515-6. PubMed ID: 6625372
[No Abstract] [Full Text] [Related]
13. Hypophosphatasia: the importance of alkaline phosphatase in bone mineralization.
Jaruratanasirikul S; Chanvitan P
J Med Assoc Thai; 1999 Dec; 82(12):1268-72. PubMed ID: 10659574
[TBL] [Abstract][Full Text] [Related]
14. Hereditary orotic aciduria. I. A new case with family studies.
Rogers LE; Warford LR; Patterson RB; Porter FS
Pediatrics; 1968 Sep; 42(3):415-22. PubMed ID: 5677482
[No Abstract] [Full Text] [Related]
15. Congenital lethal metaphyseal chondrodysplasia: a newly recognized complex autosomal recessive disorder.
Sedaghatian MR
Am J Med Genet; 1980; 6(4):269-74. PubMed ID: 7211944
[TBL] [Abstract][Full Text] [Related]
16. [Congenital hypophosphatasia].
Terheggen HG; Wischermann A
Monatsschr Kinderheilkd; 1984 Jul; 132(7):512-22. PubMed ID: 6147751
[TBL] [Abstract][Full Text] [Related]
17. Hereditary recurrent intrahepatic cholestasis from birth.
Aagenaes O; van der Hagen CB; Refsum S
Arch Dis Child; 1968 Dec; 43(232):646-57. PubMed ID: 5702224
[No Abstract] [Full Text] [Related]
18. Acatalasemia.
Aebi H; Suter H
Adv Hum Genet; 1971; 2():143-99. PubMed ID: 4950475
[No Abstract] [Full Text] [Related]
19. Hypophosphatasia: clinical and metabolic studies.
Teree TM; Klein LR
J Pediatr; 1968 Jan; 72(1):41-50. PubMed ID: 4294575
[No Abstract] [Full Text] [Related]
20. A homoallelic Gly317-->Asp mutation in ALPL causes the perinatal (lethal) form of hypophosphatasia in Canadian mennonites.
Greenberg CR; Taylor CL; Haworth JC; Seargeant LE; Philipps S; Triggs-Raine B; Chodirker BN
Genomics; 1993 Jul; 17(1):215-7. PubMed ID: 8406453
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]