Results 171 to 180 of about 162,965 (256)

Posterior segment findings in Hunter Syndrome: Case report and review. [PDF]

Am J Ophthalmol Case Rep
Majmudar IP, Ismail HO, Dang S, Gill MK.
europepmc   +1 more source

Diverse clinical outcome of Hunter syndrome in patients with chromosomal aberration encompassing entire and partial IDS deletions: what is important for early diagnosis and counseling? [PDF]

Clin Dysmorphol, 2021
Jezela-Stanek A, Pokora P, Młynek M, Smyk M, Ziemkiewicz K, Różdżyńska-Świątkowska A, Tylki-Szymańska A.   +6 more
europepmc   +1 more source

Migration, Stretched Households and the Loneliness of Older Adults in South Africa

Population, Space and Place, Volume 32, Issue 2, March 2026.
ABSTRACT This study contributes to the literature on out‐migration and the social connectedness of older adults who remain “left behind”. It investigates the loneliness reports of older African adults in the South African context, where out‐migrants are reported as retaining membership in their household of origin.
Dorrit Posel
wiley   +1 more source

Bilateral Bow Hunter Syndrome Associated with Loss of Cervical Physiological Curvature. [PDF]

Am J Case Rep
Wang S, Bi Y, Chen Y.
europepmc   +1 more source

African Decolonial Theory: A Conversation

Antipode, Volume 58, Issue 2, 2026.
Abstract Antipode has become a key platform for engaging with decolonial and anticolonial scholarship, as well as adjacent fields such as Black geographies, Indigenous studies, Latin American feminism, and work on settler‐colonialism. African reference points in this literature, however, have been far less common, both in the journal and more broadly ...
Patricia Daley, Sabelo J. Ndlovu‐Gatsheni, Wangui Kimari, Franklin Obeng‐Odoom, Sylvia Tamale, Sybille Bauriedl, Sylvia Bawa, Inken Carstensen‐Egwuom, Grace Adeniyi‐Ogunyankin, Yousuf Al‐Bulushi, Stefan Ouma   +10 more
wiley   +1 more source

Mucopolisacaridosis (síndrome de Hunter)

Revista Cubana de Medicina Militar
Se realiza una presentación de un caso interesante, no comúnmente visto en la práctica médica, de unos de los tipos de mucopolisacaridosis, específicamente de un síndrome de Hunter. Se hace esta presentación con el objetivo de dar a conocer a estudiantes
Xidix Toirac Cabrera, Luis Corvea Hernández   +1 more
doaj  

Molecular basis of mucopolysaccharidosis type II (Hunter syndrome): first review and classification of published IDS gene variants. [PDF]

Hum Genomics
Zanetti A, D'Avanzo F, Tomanin R.
europepmc   +1 more source

MAP1B Variants Disrupt Neuronal Migration: Insights From Three Novel Families

Clinical Genetics, Volume 109, Issue 3, Page 558-563, March 2026.
Pathogenic variants in MAP1B have recently emerged as a cause of neurodevelopmental disorders characterized by intellectual disability, epilepsy, and cortical malformations, including periventricular nodular heterotopia (PVNH) and polymicrogyria (PMG).
Jessica Archer, Matt Edwards, Thomas Macdougall, Anne Baxter, Himanshu Goel   +4 more
wiley   +1 more source

Advancing clinical development for neuronopathic Hunter syndrome through a quantitatively-driven reverse translation framework. [PDF]

Clin Transl Sci
Latzman RD, Campagne O, Modi ME, Karas M, Malanga CJ, Whiteman DAH.   +5 more
europepmc   +1 more source

Divergent developmental trajectories in two siblings with neuropathic mucopolysaccharidosis type II (Hunter syndrome) receiving conventional and novel enzyme replacement therapies: A case report. [PDF]

JIMD Rep, 2021
Tomita K, Okamoto S, Seto T, Hamazaki T, So S, Yamamoto T, Tanizawa K, Sonoda H, Sato Y.   +8 more
europepmc   +1 more source