Zobrazeno 1 - 10
of 77
pro vyhledávání: '"L M, Ambani"'
Publikováno v:
Indian pediatrics. 28(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fbe15cf9208a367deeb1f76e88155ef3
https://pubmed.ncbi.nlm.nih.gov/1752685
https://pubmed.ncbi.nlm.nih.gov/1752685
Publikováno v:
Indian pediatrics. 27(9)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::93ee373fa1b34a09c6014b7706ee9866
https://pubmed.ncbi.nlm.nih.gov/2286443
https://pubmed.ncbi.nlm.nih.gov/2286443
Publikováno v:
Human Genetics. 58:184-187
Chromosomal abnormalities are an important cause of mental retardation. We studied the frequency of karyotype abnormalities in 74 mentally retarded patients selected from 306 patients referred to our clinic. Giemsa-banding was done on all cases. Addi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84541f80ed34aeb42386ad3bd6667687
https://doi.org/10.1007/bf00278708
https://doi.org/10.1007/bf00278708
Publikováno v:
Journal of Biological Chemistry. 251:6616-6623
Lysosome-free preparations of rat liver mitochondria take up hydroxo[57Co]cobalamin by a process which is dependent on mitochondrial swelling, rather than on energy or ion fluxes. The uptake system is saturable and unidirectional, leading to inside/o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50927070e5123b990a6e0dea81ed2ecb
https://doi.org/10.1016/s0021-9258(17)32990-3
https://doi.org/10.1016/s0021-9258(17)32990-3
Autor:
R. K. Chawla, P. S. Bhui, K. R. Raghavan, L. M. Ambani, S. B. Shah, S. S. Dhareshwar, P. Madon, R. P. Agarwal
Publikováno v:
The Indian Journal of Pediatrics. 50:675-677
Early amnion rupture spectrum includes a wide range of congenital anomalies, varying from a single constriction band on a digit to a grossly malformed baby. The etiology remains unknownand diagnosis is missed in mostof the cases.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0122d7a0f9df2896b56ab85ec1372ee4
https://doi.org/10.1007/bf02957738
https://doi.org/10.1007/bf02957738
Publikováno v:
The Indian journal of medical research. 73
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6d1f2b4b937f3ba7a6352476b9985ad4
https://pubmed.ncbi.nlm.nih.gov/7275230
https://pubmed.ncbi.nlm.nih.gov/7275230
Publikováno v:
Indian pediatrics. 19(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b6d7ac0af00b13a9cc9f4354ed38168a
https://pubmed.ncbi.nlm.nih.gov/7118242
https://pubmed.ncbi.nlm.nih.gov/7118242
Autor:
L M, Ambani, Z M, Patel, S S, Dhareshwar, D S, Krishnamurthy, M S, Moghe, V R, Mulye, V V, Gokarn, J J, Peter, L P, Shah, S M, Merchant
Publikováno v:
The Indian journal of medical research. 79
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::52de205a8ef63c35707120a80c624246
https://pubmed.ncbi.nlm.nih.gov/6746054
https://pubmed.ncbi.nlm.nih.gov/6746054
Publikováno v:
Clinical genetics. 18(1)
Three families are described in which trophoblastic desease occurred in one or more pregnancies in two or more sisters. The possible role of genetic factors in the etiopathogenesis of hydatidiform mole is reviewed in light of these data. We believe t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a822cec70cb03a028a82a9d7821ba8e4
https://pubmed.ncbi.nlm.nih.gov/6251988
https://pubmed.ncbi.nlm.nih.gov/6251988
Publikováno v:
Indian journal of pediatrics. 48(391)
A-20-month-old boy born to consanguineous parents was evaluated for marked delay in achievement of milestones, blond hair and irritability. Large amount of phenylketones in urine, and a plasma phenylalanine of 24 mg/dl led to the diagnosis of phenylk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea24d139c3f76e585f7f990401f1306e
https://pubmed.ncbi.nlm.nih.gov/7298095
https://pubmed.ncbi.nlm.nih.gov/7298095