Cargando…

Congenital Family Cholæmia

Detalles Bibliográficos
Autores principales:	Mackintosh, Ashley W., Falconer, A. W., Anderson, A. G.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oliver and Boyd 1911
Materias:	Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5253960/

Ejemplares similares

Lectures on Diseases of the Nervous System
por: Mackintosh, Ashley W.
Publicado: (1904)

Congenital Family Steatorrhea
Publicado: (1914)

Familial Focal Congenital Hyperinsulinism
por: Ismail, Dunia, et al.
Publicado: (2011)

Familial co-occurrence of congenital heart defects follows distinct patterns
por: Ellesøe, Sabrina G, et al.
Publicado: (2018)

Notes on Some Cases of Regular Slow Pulse
por: Falconer, A. W.
Publicado: (1910)

Dyspituitarism
por: Falconer, A. W.
Publicado: (1913)

Further Note on a Case of Dyspituitarism
por: Falconer, A. W.
Publicado: (1914)

CONGENITAL CYSTIC KIDNEY AND LIVER WITH FAMILY TENDENCY
por: Bunting, C. H.
Publicado: (1906)

Genome sequencing in families with congenital limb malformations
por: Elsner, Jonas, et al.
Publicado: (2021)

Higher congenital transmission rate of Trypanosoma cruzi associated with family history of congenital transmission
por: Danesi, Emmaría, et al.
Publicado: (2020)

Novel human CRYGD rare variant in a Brazilian family with congenital cataract
por: de Figueirêdo, Eugênio Santana, et al.
Publicado: (2011)

Aneurysm of the Hepatic Artery
por: Dean, George, et al.
Publicado: (1912)

Nonsyndromic Familial Congenital Lower Lip Pits
por: Hambire, Chaitali, et al.
Publicado: (2019)

Congenital Atresia of the Œsophagus
por: Gailey, A. A. H., et al.
Publicado: (1951)

Mutation analysis of two families with inherited congenital cataracts
por: LIANG, CHANG, et al.
Publicado: (2015)

Molecular Genetic Analysis of Ukrainian Families with Congenital Cataracts
por: Jiao, Xiaodong, et al.
Publicado: (2022)

Severe congenital neutropenia in a multigenerational family with a novel neutrophil elastase (ELANE) mutation
por: van de Vosse, Esther, et al.
Publicado: (2010)

Mutational screening of Indian families with hereditary congenital cataract
por: Ponnam, Surya Prakash Goud, et al.
Publicado: (2013)

Mutations in FYCO1 identified in families with congenital cataracts
por: Iqbal, Hira, et al.
Publicado: (2020)

Congenitally corrected transposition
por: Wallis, Gonzalo A, et al.
Publicado: (2011)

Case of Congenital Cephalocele
por: Peck, W. A.
Publicado: (1856)

A Novel ABCA12 Mutation in Two Families with Congenital Ichthyosis
por: Walsh, D. M., et al.
Publicado: (2012)

Farmacología y terapéutica
por: Falconer, Mary W
Publicado: (1972)

The CHIP-Family study to improve the psychosocial wellbeing of young children with congenital heart disease and their families: design of a randomized controlled trial
por: van der Mheen, Malindi, et al.
Publicado: (2018)

Anti-tumour activity of afatinib, an irreversible ErbB family blocker, in human pancreatic tumour cells
por: Ioannou, N, et al.
Publicado: (2011)

Congenital Hyperkeratosis
por: Foggie, W. E.
Publicado: (1922)

Novel mutations in CRYGD are associated with congenital cataracts in Chinese families
por: Yang, Guoxing, et al.
Publicado: (2016)

Novel mutations in CRYGC are associated with congenital cataracts in Chinese families
por: Zhong, Zilin, et al.
Publicado: (2017)

Screening Children with a Family History of Central Congenital Hypoventilation Syndrome
por: Emanuel, Hina, et al.
Publicado: (2020)

Families’ Experiences of Continuous Glucose Monitoring in the Management of Congenital Hyperinsulinism: A Thematic Analysis
por: Auckburally, Sameera Hannah, et al.
Publicado: (2022)

Mutation analysis of 12 genes in Chinese families with congenital cataracts
por: Sun, Wenmin, et al.
Publicado: (2011)

Social impact on families of children with complex congenital heart disease
por: Almesned, Sulaiman, et al.
Publicado: (2013)

Mutation screening of crystallin genes in Chinese families with congenital cataracts
por: Zhuang, Jianfu, et al.
Publicado: (2019)

Clinical and genetic findings in Chinese families with congenital ectopia lentis
por: Liu, Xin, et al.
Publicado: (2023)

“This Is What Family Does”: The Family Experience of Caring for Serious Illness
por: Anderson, Eric W., et al.
Publicado: (2017)

Evaluation of a psychosocial education program for families with congenital adrenal hyperplasia
por: Mitchelhill, I, et al.
Publicado: (2013)

Behavioral effects of congenital ventromedial prefrontal cortex malformation
por: Boes, Aaron D, et al.
Publicado: (2011)

High Familial Recurrence of Congenital Heart Defects in Laterality Defects Patients: An Evaluation of 184 Families
por: Hu, Huifang, et al.
Publicado: (2021)

"Simple Persistent" and "Congenital Persistent" Jaundice, Family Biliary Cirrhosis, and Family Tendency to Jaundice
por: Weber, F. Parkes
Publicado: (1903)

Congenital Epulis
por: Middleton, D. Stewart, et al.
Publicado: (1933)

Cannot write session to /tmp/vufind_sessions/sess_3qn7radovbdfe8a98s70fuqkbq