Results 31 to 40 of about 433 (176)

Addressing Gaps in Butterfly Population Monitoring to Catalyze Global Insect Conservation

Conservation Letters, Volume 19, Issue 2, March/April 2026.
ABSTRACT The conservation community sorely lacks a global indicator of change in insect populations. Given widespread insect declines, addressing this gap is key for conservation and policy targets. We suggest that butterfly monitoring programs can serve as the foundation for an effective global network of insect monitoring.
F. Riva, R. Schmucki, R. Cooke, M. Balalaikins, J. M. Barea‐Azcón, D. N. Basu, M. Böhm, T. C. Bonebrake, S. Chowdhury, O. Comay, A. O. Debrot, A. J. Dolezal, E. E. Dyer, B. Fontaine, Z. F. Fric, R. Girotra, N. J. B. Isaac, K. R. Nagesh, E. Kühn, K. Kunte, A. S. Kutt, M. Kuussaari, M. Larivee, N. Legall, V. V. Lien, H. M. Madden, D. Maes, S. P. McGaffin, L. McRae, X. Mestdagh, M. L. Munguira, M. Musche, H. I. Mynott, V. Nawge, G. Pe'er, L. B. Pettersson, J. Pippen, L. Ries, T. Roth, M. Šašić, J. Settele, C. Sevilleja, S. Sheikh, M. Sielezniew, R. Solis, C. Stefanescu, N. Titeux, E. Tzirkalli, A. Ubach, C. A. M. van Swaay, A. Walker, B. A. Woodcock, David B. Roy   +52 more
wiley   +1 more source

Síndrome de Waardenburg: las discapacidades y el aspecto físico, su vinculación con el rendimiento académico y las relaciones sociales Waardenburg's syndrome: disabilities and physical features, association with academic achievement and social relations

Revista de Ciencias Médicas de Pinar del Río, 2012
Introducción: el síndrome de Waardenburg es una entidad infrecuente, que cursa con cierto grado de discapacidad cuando aparece la hipoacusia neurosensorial y la discapacidad visual; se ha detectado en el municipio Sandino en Pinar del Río, una familia ...
Fidel Castro Pérez, José Guillermo Sanabria Negrín, Marisela Torres Capote, Rolando Jesús Iviricu Tielves, Heidy González Serrano   +4 more
doaj  

Pigment Anomalies Encountered in the Transkei [PDF]

, 2018
The function and production of pigmentation are discussed in relation to pigment anomalies encountered in the ...
Rose, E.F.
core   +1 more source

Genetic Pigmentary Disorders: From Molecular Mechanisms to Clinical Manifestations

The Journal of Dermatology, Volume 53, Issue 2, Page 169-179, February 2026.
ABSTRACT Genetic pigmentary disorders represent a diverse group of genetic conditions characterized by alterations in melanin production and transport and melanocyte development, resulting from single‐gene pathological variants. These disorders encompass both hypopigmentary and hyperpigmentary phenotypes, affecting not only skin pigmentation but also ...
Ken Okamura, Tamio Suzuki
wiley   +1 more source

Waardenburg syndrome

Kerala Journal of Ophthalmology, 2018
Waardenburg syndrome is a rare genetic disorder with at least 1,400 cases has been reported in medical lecture.In waardenburg syndrome a patient presents with hypopigmented areas of skin,white forelock of hairs,difference in the colour of both iris and some associated conditions like hirschsprung disease,malformation of upper limbs as well as certain ...
Anubhav Chauhan, Shveta Chauhan
openaire   +4 more sources

A case of Waardenburg syndrome and aganglionosis

The Turkish Journal of Pediatrics, 1992
Waardenburg's syndrome is characterized by a broad nasal root, pigmentation disturbance and congenital deafness while aganglionosis is described as the partial or complete lack of ganglion cells in the alimentary tract.
E Aritürk, N Tosyali, N Aritürk
doaj  

Últimos retos en el tratamiento de la catarata congénita [PDF]

, 2022
La descripció de la cataracta congènita és una opacitat de la lent ocular que apareix en el part o durant la primera infància, és una malaltia rara i sovint desconeguda, però a excepció d'altres raons associades amb ella que inclouen: genètica ...
Amro, Shaden Khalil B.
core  

Pathology Seen in Myenteric Plexus in Two Subjects With Waardenburg Syndrome

Neurogastroenterology &Motility, Volume 37, Issue 12, December 2025.
Ganglion cells immunohistochemically labeled with pan‐neuronal marker HuC/D in sections from ileum. Note the different number of stained cells in the myenteric plexus. A, control subject, B, patient with SOX10 mutation (hypoganglionosis) C, patient with EDN3 mutation (aganlionosis). Both patients diagnosed with Waardenburg syndrome type 4 including gut
Björn Ersson, Elisabet Gustafson, Johan Danielson, Irina Alafuzoff   +3 more
wiley   +1 more source

The Diverse Genetic Landscape of Hearing Impairment in South African Families

Clinical Genetics, Volume 108, Issue 5, Page 511-520, November 2025.
South African Families with Nonsyndromic (N = 24) and Syndromic Hearing Impairment (N = 21) with ≥ 2 affected members were analyzed. The underlying etiology was uncovered using exome and Sanger sequencing for 31 of these families. ABSTRACT To elucidate the genetic etiology of hearing impairment (HI) in South Africa, 45 nonsyndromic HI (NSHI) and ...
Thashi Bharadwaj, Anushree Acharya, Noluthando Rearabetswe Manyisa, Elvis Twumasi Aboagye, Ramses Peigou Wonkam, Lettilia Xhakaza, Kalinka Popel, Carmen de Kock, Isabelle Schrauwen, Ambroise Wonkam, Suzanne M. Leal   +10 more
wiley   +1 more source

Síndrome de Waardenburg: clasificación clínica de una familia Waardenburg's syndrome: clinical classification of a family

Revista de Ciencias Médicas de Pinar del Río, 2012
Introducción: El síndrome de Waardenburg (SW) es una entidad infrecuente, hereditaria, que cursa con cierto grado de discapacidad cuando aparece la hipoacusia neurosensorial y su cuadro clínico no está completamente definido.
Fidel Castro Pérez, José Guillermo Sanabria Negrín, Reinaldo Menéndez García   +2 more
doaj