Výsledky vyhledávání - "Poor feeding"

Akademický článek

Typology of Red Maradi goat farming systems in Benin based on farmers’ survey

Autor: Fréjus T.A. Zinsou, Pascal A. Olounladé, Géorcelin G. Alowanou, Adam D. Adenilé, Hyppolite A. Sèdédji, Eunice A.F. Bamigbochey, Sylvie M. Hounzangbé-Adoté

Publikováno v: Heliyon, Vol 10, Iss 22, Pp e40256- (2024)

Goat farming contributes to the family economy, sustainable livelihoods and reduces poverty in rural households in Sub-Sahara areas. Also called “Poor man's cow”, Red Maradi goat is a Niger-originated dairy goat introduced in Benin by the West Af

Externí odkaz: https://doaj.org/article/9db09364345c408297d84f2f69708ed0

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Akademický článek

Typology of Red Maradi goat farming systems in Benin based on farmers’ survey

Autor: Zinsou, Fréjus T.A. ^{a, b}, Olounladé, Pascal A. ^{a, b, ⁎}, Alowanou, Géorcelin G. ^{a, c}, Adenilé, Adam D. ^{a, d}, Sèdédji, Hyppolite A. ^d, Bamigbochey, Eunice A.F. ^d, Hounzangbé-Adoté, Sylvie M. ^{a, d}

Publikováno v: In Heliyon 30 November 2024 10(22)

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Akademický článek

Transcutaneous auricular vagus nerve stimulation may benefit from the addition of N-acetylcysteine to facilitate motor learning in infants of diabetic mothers failing oral feeds

Autor: Dorothea D. Jenkins, Sandra S. Garner, Alyssa Brennan, Jessica Morris, Kate Bonham, Lauren Adams, Sally Hunt, Hunter Moss, Bashar W. Badran, Mark S. George, Donald B. Wiest

Publikováno v: Frontiers in Human Neuroscience, Vol 18 (2024)

ObjectiveThis study aims to determine if pretreating with enteral N-acetylcysteine (NAC) improves CNS oxidative stress and facilitates improvement in oromotor skills during transcutaneous auricular nerve stimulation (taVNS) paired with oral feedings

Externí odkaz: https://doaj.org/article/1a74cf9928584cb1adc0fccdc13aae31

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Akademický článek

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Akademický článek

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Akademický článek

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Causes, Types, Symptoms and Diagnosis of Methyl Melonic Acidemia (MMA), Common Symptoms of Methyl Malonic Acid (MMA) and Homocysteine (HMA -HCY0, Differential Diagnosis of Methyl Malonic Acidemia (MMA), Treatment of Methyl Melonyl Acidemia

Autor: Vinayasree. C, Mohan Naidu. K, Muralinath. E, Amrutham Sandeep, Venkat Naveen. A, Guruprasad. M, Sravani Pragna. K

Methylmalonic acidemia (MMA) is a rare inherited metabolic disorder manifested by impaired metabolism of certain amino acids and fatty acids. It occurs by a deficiency of the enzyme methylmalonyl-CoA mutase, which leads to the collection of toxic lev

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bd3cd6569dacfc79ce47c339bf54ed6

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Cold steel supraglottoplasty for severe laryngomalacia in infants

Autor: Arun Alexander, Soorya Pradeep

Publikováno v: BMJ case reports. 14(7)

A 9-month-old female baby was brought to the emergency room (ER) by her parents with reports of noisy breathing, poor feeding, inadequate weight gain and intermediate cyanotic spells noticed for the past month. She was a full-term baby weighing 2.8 k

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b0c602a5197a18f2501390561af1e48
https://pubmed.ncbi.nlm.nih.gov/34290012

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Types and Causes of Citrullinemia Type I, Type II, Symptoms of Citrullinemia Type I, Type II, Diagnosis of Citrullinemia, Clinical Evaluation of Citrullinemia and Treatment of Cutrullinemia

Autor: Vinayasree.C, Naidu.K, Mohan, Muralinath.E, Amrutham Sandeep, Venkat Naveen . A, Guruprasad.M, Sravani Pragna.K

Citrullinemia is a rare genetic disorder that affects the metabolism of the amino acid arginine. It is manifested by the collection of citrulline, a toxic substance, in the blood and tissues due to the deficiency or malfunctioning of an enzyme called

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f0ca18017d3caf6e26906d35158f61c

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Symptoms, Treatment, Complications as well as Prognosis of Classic Maple Syrup Urine Disease (MSUD), Metabolic Instability, Neurological Complications and Treatment Of Intermediate MSUD, Case Studies as well as Success Stories of Thiamine Responsive MSUD

Autor: Vinayasree. C, Mohan Naidu. K, Muralinath. E, Amrutham Sandeep, Venkat Naveen. A, Guruprasad. M, Sravani Pragna. K

Maple Syrup Urine Disease (MSUD) is a rare inherited metabolic disorder manifested by the impaired catabolism of certain amino acids. This disorder results in the collection of toxic substances in the body, leading to a range of symptoms and complica

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71e14a98f76d43e83cfdc5d1984ce5c6

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