phenylephrine-hydrochloride and Hepatitis

phenylephrine-hydrochloride has been researched along with Hepatitis* in 2 studies

Other Studies

2 other study(ies) available for phenylephrine-hydrochloride and Hepatitis

Article	Year
Johanson-Blizzard syndrome: hepatic and hematological features with novel genotype. Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology, 2014, Volume: 33, Issue:1 Johanson-Blizzard syndrome (JBS); (OMIM: 243800) presents with features of malabsorption and dysmorphic features with onset of symptoms in infantile age group. The disorder was first described in the year 1971 with report of the first Indian case in 2004. We discuss two rare phenotypes (hepatitis and anemia) in a molecularly confirmed case of JBS. Topics: Anemia; Anus, Imperforate; Chromosomes, Human, Pair 15; Ectodermal Dysplasia; Genes, Recessive; Genetic Testing; Genotype; Growth Disorders; Hearing Loss, Sensorineural; Hematologic Tests; Hepatitis; Humans; Hypothyroidism; Infant; Intellectual Disability; Male; Mutation; Nose; Pancreatic Diseases; Phenotype; Ubiquitin-Protein Ligases	2014
[Malformations in otorhinolaryngology. Genetic report]. Archiv fur klinische und experimentelle Ohren- Nasen- und Kehlkopfheilkunde, 1972, Volume: 202, Issue:2 Topics: Abnormalities, Drug-Induced; Abnormalities, Multiple; Child; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 16-18; Congenital Abnormalities; Deafness; Down Syndrome; Ear; Ear, External; Hepatitis; Humans; Larynx; Male; Mutation; Nose; Thalidomide; Trisomy	1972

Article

Year

Johanson-Blizzard syndrome: hepatic and hematological features with novel genotype.

Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology, 2014, Volume: 33, Issue:1

Johanson-Blizzard syndrome (JBS); (OMIM: 243800) presents with features of malabsorption and dysmorphic features with onset of symptoms in infantile age group. The disorder was first described in the year 1971 with report of the first Indian case in 2004. We discuss two rare phenotypes (hepatitis and anemia) in a molecularly confirmed case of JBS.

Topics: Anemia; Anus, Imperforate; Chromosomes, Human, Pair 15; Ectodermal Dysplasia; Genes, Recessive; Genetic Testing; Genotype; Growth Disorders; Hearing Loss, Sensorineural; Hematologic Tests; Hepatitis; Humans; Hypothyroidism; Infant; Intellectual Disability; Male; Mutation; Nose; Pancreatic Diseases; Phenotype; Ubiquitin-Protein Ligases

2014

[Malformations in otorhinolaryngology. Genetic report].

Archiv fur klinische und experimentelle Ohren- Nasen- und Kehlkopfheilkunde, 1972, Volume: 202, Issue:2

Topics: Abnormalities, Drug-Induced; Abnormalities, Multiple; Child; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 16-18; Congenital Abnormalities; Deafness; Down Syndrome; Ear; Ear, External; Hepatitis; Humans; Larynx; Male; Mutation; Nose; Thalidomide; Trisomy

1972