Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ashish Lothe"'
Publikováno v:
Indian Journal of Child Health. :15-19
Background: Assessment of gestational age (GA) based on the last date of menstrual period is often inaccurate. Scores to predict GA of newborns are difficult to use particularly by health workers. An accurate, easy to use the method of assessing GA,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::103f8f73de69e010c8136586eb7faf42
https://doi.org/10.32677/ijch.2018.v05.i01.004
https://doi.org/10.32677/ijch.2018.v05.i01.004
Publikováno v:
Indian Journal of Child Health. :340-344
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b18c304753a678c7b6e467d97474a3c4
https://doi.org/10.32677/ijch.2018.v05.i05.007
https://doi.org/10.32677/ijch.2018.v05.i05.007
Publikováno v:
Journal of Paediatrics and Child Health. 47:550-553
Aim: To illustrate, via case histories, the importance of laboratory investigations for the early diagnosis and management of metabolic bone disease (MBD). Methods: We report three cases of extreme premature infants with MBD. Results: These three inf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::680bee5441440f7513f8b7a425c045f9
https://doi.org/10.1111/j.1440-1754.2011.02019.x
https://doi.org/10.1111/j.1440-1754.2011.02019.x
Publikováno v:
Journal of Hematology & Thromboembolic Diseases.
Sickle cell disease (SCD) is one of the most common monogenic diseases worldwide. Although there have been some advances in the management of SCD, much remains to be learned about the mechanisms underlying the wide phenotypic diversity of the disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f550b80edb909bc7aa1e2a27c6af3cf
https://doi.org/10.4172/2329-8790.1000224
https://doi.org/10.4172/2329-8790.1000224
Publikováno v:
Journal of paediatrics and child health. 47(8)
To illustrate, via case histories, the importance of laboratory investigations for the early diagnosis and management of metabolic bone disease (MBD).We report three cases of extreme premature infants with MBD.These three infants had several risk fac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9995489dc126183f7b9b336d6b9223b0
https://pubmed.ncbi.nlm.nih.gov/21392146
https://pubmed.ncbi.nlm.nih.gov/21392146
Autor:
Leena Dhande, Ashish Lothe
Publikováno v:
Sri Lanka Journal of Child Health. 44:171
Griscelli syndrome (GS) is rare autosomal recessive disorder with pigmentary dilution, immunodeficiency and neurological involvement1,2. We report a child with classical features of GS and pathognomonic histopathological features of skin and hair. Sr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a12decdebf3ef4efc3799284240e74eb
https://doi.org/10.4038/sljch.v44i3.8019
https://doi.org/10.4038/sljch.v44i3.8019