Results 51 to 60 of about 1,444,136 (141)
Mutations in the Human ROBO1 Gene in Pituitary Stalk Interruption Syndrome
International audiencePituitary stalk interruption syndrome (PSIS) is characterized by a thin or absent pituitary stalk usually in association with an ectopic posterior pituitary and hypoplasia/aplasia of the anterior pituitary.
Raja Brauner +9 more
core +1 more source
Abstracts submitted to the ‘EACR 2025 Congress: Innovative Cancer Science’, from 16–19 June 2025 and accepted by the Congress Organising Committee are published in this Supplement of Molecular Oncology, an affiliated journal of the European Association for Cancer Research (EACR).
wiley +3 more sources
Background Pituitary stalk interruption syndrome (PSIS) is a rare disease associated with different level of anterior pituitary hormone deficiency resulting with a variety of clinical manifestations which could limit exercise capacity.
Wei Hung Sung +3 more
doaj +1 more source
Polysaccharides play a pivotal role in the development of safe and healthy foods. They ameliorate fatigue, preserve the microflora of the gastrointestinal tract, and provide health for the gut in living organisms. These biopolymers are applied for the fabrication of breakthrough drug delivery systems and potential platforms in regenerative medicine ...
M V N L Chaitanya +14 more
wiley +1 more source
Whole-Exome Sequencing Identifies Homozygous GPR161 Mutation in a Family with Pituitary Stalk Interruption Syndrome [PDF]
Erdin, Serkan/0000-0001-6587-2625; Yaykasli, Kursat/0000-0001-7550-6370; Yaykasli, Emine/0000-0001-6471-0106; Gambin, Tomasz/0000-0002-0941-4571WOS: 000353281300033PubMed: 25322266Context: Pituitary stalk interruption syndrome (PSIS) is a rare ...
Yaykaşlı, Kürşat Oğuz +24 more
core +1 more source
Development of the neurohypophysis: A major neuroendocrine interface
Abstract The neurohypophysis is a major central neuroendocrine interface regulating reproductive functions and water homeostasis. Distinct neurovascular cell types interact via evolutionarily conserved signaling molecules in the developing neurohypophysis, providing a model system for studying principles in neuroendocrine interface morphogenesis.
Athul R. Ramesh +5 more
wiley +1 more source
A Rare Cause of Pituitary Deficiency: Pituitary Stalk Interruption Syndrome and Magnetic Resonance Imaging Findings [PDF]
Pituitary stalk interruption syndrome is a rare disease characterized by a deficiency of adenohypophyseal hormones. Clinical presentation usually occurs in childhood or in the second decade of life. The severity of hormonal deficiency is variable. It may
Atilla Hikmet Çilengir +8 more
core +2 more sources
Clinical characteristics of 55 patients with PSIS.
ND: not documented. F: female. M: male. SDS: standard deviation scores. PSIS: Pituitary stalk interruption syndrome.
Jianming Ba (288865) +19 more
core +1 more source
Digenic Inheritance of PROKR2 and WDR11 Mutations in Pituitary Stalk Interruption Syndrome [PDF]
Context: Pituitary stalk interruption syndrome (PSIS, ORPHA95496) is a congenital defect of the pituitary gland characterized by the triad of a very thin/interrupted pituitary stalk, an ectopic (or absent) posterior pituitary gland, and hypoplasia or ...
Kim, YJ +13 more
core +1 more source
Objectives To determine the importance of serum prolactin (PRL) in the detection of pituitary stalk interruption syndrome (PSIS) in children with multiple pituitary hormone deficiency (MPHD).
Eren, Erdal +6 more
core +1 more source

