Zobrazeno 1 - 10
of 10
pro vyhledávání: '"M N, KAY"'
Publikováno v:
Pediatrics. 22:319-328
A case of Sturge-Weber's disease, confirmed by necropsy, in a female 2 3/12 years old, is presented. This case, aside from its rarity, is noteworthy in that it is confirmed by necropsy, that the facial lesion is bilateral while the brain lesion is un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9430efc4108e2aca7b8f15d190aeb3ce
https://doi.org/10.1542/peds.22.2.319
https://doi.org/10.1542/peds.22.2.319
Autor:
M. N. Kay, L. W. Falkinburg
Publikováno v:
The Journal of Pediatrics. 54:162-169
Summary 1. A case of Peutz-Jeghers syndrome, in a 5-year-old boy, one of the youngest on record, is added to the pediatric literature. 2. The various elements that comprisethis unusual symptom complex are reviewed, and various therapeutic and prophyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb9686ca4765bca65375353866db0870
https://doi.org/10.1016/s0022-3476(59)80058-5
https://doi.org/10.1016/s0022-3476(59)80058-5
Publikováno v:
Pediatrics. 22(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3e95f2fac7d39cde2f5edf89e097e6c4
https://pubmed.ncbi.nlm.nih.gov/13578518
https://pubmed.ncbi.nlm.nih.gov/13578518
Autor:
L W, FALKINBURG, M N, KAY
Publikováno v:
American practitioner and digest of treatment. 10(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cf6ad56f7bdb31b7644fca2ad6b030bf
https://pubmed.ncbi.nlm.nih.gov/13627404
https://pubmed.ncbi.nlm.nih.gov/13627404
Autor:
L W, FALKINBURG, M N, KAY
Publikováno v:
Archives of pediatrics. 79
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6523c31378d2fbdef42ce74f2c3b8476
https://pubmed.ncbi.nlm.nih.gov/13891455
https://pubmed.ncbi.nlm.nih.gov/13891455
Autor:
L W, FALKINBURG, M N, KAY
Publikováno v:
The Journal of pediatrics. 54(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1e53c7c060708423dac8f36f08dd5852
https://pubmed.ncbi.nlm.nih.gov/13621362
https://pubmed.ncbi.nlm.nih.gov/13621362
Publikováno v:
A.M.A. Journal of Diseases of Children. 99:86
Crossed renal ectopia with fusion is a very rare condition, and crossed ectopia without fusion is much rarer. Review of the literature since the appearance of Wilmer's1excellent and comprehensive article in 1938 shows that this condition has been rep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ba26fe44970a2485ad613b78237baa0
https://doi.org/10.1001/archpedi.1960.02070030088015
https://doi.org/10.1001/archpedi.1960.02070030088015
Publikováno v:
Archives of Pediatrics & Adolescent Medicine. 88:458
GALACTOSEMIA,* which is frequently familial, is manifested by vomiting, diarrhea, poor weight gain, malnutrition, and the presence of albumin and galactose in the urine while lactose is present in the diet. Jaundice, mental retardation, and cataracts
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7870601812bf2c4cc91eb03d9e17e750
https://doi.org/10.1001/archpedi.1954.02050100460005
https://doi.org/10.1001/archpedi.1954.02050100460005
Autor:
Harry J. Cohen, M. N. Kay
Publikováno v:
Archives of Pediatrics & Adolescent Medicine. 62:606
The syndrome of associated facial hemangioma and intracranial lesion is characterized by the presence of two outstanding signs: (1) a facial port wine nevus (fig. 1) present at birth, which follows the distribution of one or more branches of the fift
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9f94140e02faf5e8562d700b5aea535
https://doi.org/10.1001/archpedi.1941.02000150130016
https://doi.org/10.1001/archpedi.1941.02000150130016
Publikováno v:
Journal of the American Medical Association. 155:1228
Despite the grave prognosis usually associated with nephroblastoma (Wilms' tumor), numerous reports have appeared in the literature concerning long survival of the patient after operation. Silver 1 presented a series of 18 patients, 10 of whom were s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6329469def69131afc96833cfd12960
https://doi.org/10.1001/jama.1954.73690320001010
https://doi.org/10.1001/jama.1954.73690320001010