Works matching DE "CAFE-au-Lait spots (Disease)"

Results: 52

Brain MRI analysis of six patients with neurofibromatosis type 1.

Published in:

Chinese Journal of Contemporary Neurology & Neurosurgery, 2019, v. 19, n. 3, p. 205, doi. 10.3969/j.issn.1672-6731.2019.03.011

By:

ZHU Hua-qian;
LI Lei;
JIN Feng;
OUYANG Yi

Publication type:

Article

A Water-Damaged Home and Health of Occupants: A Case Study.

Published in:

2012

By:

Thrasher, Jack Dwayne;
Gray, Michael R.;
Kilburn, Kaye H.;
Dennis, Donald P.;
Yu, Archie

Publication type:

Case Study

McCune Albright syndrome in association with excessive GH secretion: case report.

Published in:

Türk Pediatri Arşivi, 2015, v. 50, n. 2, p. 114, doi. 10.5152/tpa.2015.615

By:

Özsu, Elif;
Mutlu, Gül Yeşiltepe;
Çizmecioğlu, Filiz Mine;
Hatun, Şükrü

Publication type:

Article

Plexiform neurofibromatosis type 1.

Published in:

2016

By:

Sharma, Surendra K.;
Sharma, Abhishek

Publication type:

Case Study

Mongolian spots combined with halo-like disappearance surrounding café au lait spots.

Published in:

2018

By:

Temel, Aslı Bilgiç;
Bassorgun, Cumhur Ibrahim;
Nur, Banu;
Alpsoy, Erkan

Publication type:

Case Study

Plexiform neurofibromatosis of the liver: an extremely rare case.

Published in:

Gastroenterology & Hepatology from Bed to Bench, 2022, v. 15, n. 3, p. 282, doi. 10.22037/ghfbb.v15i3.2047

By:

Gharekhanloo, Farideh;
Lorestani, Saba;
Khazaei, Salman

Publication type:

Article

Evaluation of Clinical and Laboratory Features of Patients with Ataxia-Telangiectasia.

Published in:

Asthma Allergy Immunology / Astim Allerji Immunoloji, 2023, v. 21, n. 1, p. 3, doi. 10.21911/aai.006

By:

KILIC, Mehmet;
GUNBEY, Omer;
TASKIN, Erdal;
DAG, Bunyamin;
KUCUK, Elif;
GUNBEY, Fatma Betul;
SEN, Askin

Publication type:

Article

Spontaneous Near Fatal Hemorrhage into Neurofibromatosis Type 1 Lesion in the Scalp.

Published in:

Oman Medical Journal, 2022, v. 37, n. 3, p. 19, doi. 10.5001/omj.2022.02

By:

Stephen, Edwin;
Kariyattil, Rajeev;
Mittal, Alok;
Al-Azri, Faisal;
Al-Wahaibi, Khalifa

Publication type:

Article

Legius syndrome: case report and review of literature.

Published in:

Italian Journal of Pediatrics, 2015, v. 41, n. 1, p. 1, doi. 10.1186/s13052-015-0115-9

By:

Benelli, Elisa;
Bruno, Irene;
Belcaro, Chiara;
Ventura, Alessandro;
Berti, Irene

Publication type:

Article

Fibrous dysplasia and McCune-Albright syndrome: A case report with review of literature on the rehabilitation approach.

Published in:

Turkish Journal of Physical Medicine & Rehabilitation (2587-1250), 2023, v. 69, n. 2, p. 252, doi. 10.5606/tftrd.2023.8815

By:

Aslan, Sefa Gümrük;
Tezel, Kutay;
Ordu-Gökkaya, N. Kutay

Publication type:

Article

Association of Piebaldism, Multiple Café-au-lait Macules, and Intertriginous Freckling: Clinical Evidence of a Common Pathway between KIT and Sprouty-Related, Ena/Vasodilator-Stimulated Phosphoprotein Homology-1 Domain Containing Protein 1 (SPRED1)

Published in:

Pediatric Dermatology, 2013, v. 30, n. 3, p. 379, doi. 10.1111/j.1525-1470.2012.01858.x

By:

Chiu, Yvonne E.;
Dugan, Stefanie;
Basel, Donald;
Siegel, Dawn H.

Publication type:

Article

Café-au-lait Spots and Cleft Palate: Not a Chance Association.

Published in:

Cleft Palate Craniofacial Journal, 2024, v. 61, n. 11, p. 1932, doi. 10.1177/10556656231188205

By:

Yamada, Mamiko;
Tanito, Katsumi;
Suzuki, Hisato;
Nakato, Daisuke;
Miya, Fuyuki;
Takenouchi, Toshiki;
Kosaki, Kenjiro

Publication type:

Article

Bilateral Cleft Lip and Palate in Ring Chromosome 7 Syndrome: A Case Report and Review of Clinical Characteristics.

Published in:

Cleft Palate Craniofacial Journal, 2024, v. 61, n. 3, p. 527, doi. 10.1177/10556656221149243

By:

Bangun, Kristaninta;
Kreshanti, Prasetyanugraheni;
Tania, Vika;
Ariani Aswin, Yulia;
Menna, Clara;
Aurino, Leorca

Publication type:

Article

Painless Loss of Vision as The First Presentation of Undiagnosed Neurofibromatosis 1 in A Child.

Published in:

2015

By:

PAUL, Siba Prosad;
AHMED, Shameem

Publication type:

Case Study

Dermatologic manifestations in paediatric neurofibromatosis type 2: a cross sectional descriptive multicentric study.

Published in:

2022

By:

Legoupil, S.;
Bessis, D.;
Picard, F.;
Mallet, S.;
Mazereeuw, J.;
Phan, A.;
Dupin-Deguine, D.;
Kalamarides, M.;
Chiaverini, C.;
Research Group of the French Society of Paediatric Dermatology

Publication type:

journal article

Rumień trwały -- zjawiska patogenetyczne i różnorodność obrazu klinicznego.

Published in:

Dermatology Review / Przeglad Dermatologiczny, 2012, v. 99, n. 3, p. 252

By:

Tekely, Emilia;
Kądziela-Wypyska, Grażyna;
Chodorowska, Grażyna

Publication type:

Article

Clinical and endocrine characteristics and genetic analysis of Korean children with McCune-Albright syndrome: a retrospective cohort study.

Published in:

2016

By:

Eun-Kyung Cho;
Jinsup Kim;
Aram Yang;
Chang-Seok Ki;
Ji-Eun Lee;
Sung Yoon Cho;
Dong-Kyu Jin;
Cho, Eun-Kyung;
Kim, Jinsup;
Yang, Aram;
Ki, Chang-Seok;
Lee, Ji-Eun;
Cho, Sung Yoon;
Jin, Dong-Kyu

Publication type:

journal article

Copy number variants and rasopathies: germline KRAS duplication in a patient with syndrome including pigmentation abnormalities.

Published in:

2016

By:

Gilbert-Dussardier, Brigitte;
Briand-Suleau, Audrey;
Laurendeau, Ingrid;
Bilan, Frédéric;
Cavé, Hélène;
Verloes, Alain;
Vidaud, Michel;
Vidaud, Dominique;
Pasmant, Eric

Publication type:

Letter

Optic nerve glioma in neurofibromatosis: Radiological clues to diagnosis in a young child.

Published in:

Journal of Pediatric Neurosciences, 2021, v. 16, n. 3, p. 264, doi. 10.4103/jpn.JPN_189_20

By:

Patel, Harsh;
Chakrabarty, Biswaroop;
Dubey, Rachna;
Kumar, Atin;
Gulati, Sheffali

Publication type:

Article

Möbius syndrome associated with neurofibromatosis Type 1: A rare co-occurrence.

Published in:

Journal of Pediatric Neurosciences, 2015, v. 10, n. 2, p. 172, doi. 10.4103/1817-1745.159205

By:

Sharma, Ankush;
Gupta, Nitin;
Talwar, Tejinder;
Gupta, Munish

Publication type:

Article

Café-Au-Lait Macules in Neurofibromatosis Type 1: Birthmark or Biomarker?

Published in:

Cancers, 2025, v. 17, n. 9, p. 1490, doi. 10.3390/cancers17091490

By:

Santangelo, Andrea;
Chelleri, Cristina;
Tomasino, Marco;
Pasquinucci, Mattia;
Cappozzo, Francesca;
Striano, Pasquale;
Diana, Maria Cristina;
Scala, Marcello

Publication type:

Article

Cutaneous Findings in Neurofibromatosis Type 1.

Published in:

Cancers, 2021, v. 13, n. 3, p. 463, doi. 10.3390/cancers13030463

By:

Ozarslan, Bengisu;
Russo, Teresa;
Argenziano, Giuseppe;
Santoro, Claudia;
Piccolo, Vincenzo

Publication type:

Article

Deletion 21pterq22.11: Report of a Patient with Dysmorphic Features, Hypertonia, and Café-au-Lait Macules and Review of the Literature.

Published in:

2018

By:

Malinverni, Andréa C.M.;
Yamashiro Coelho, Érika M.;
Chen, Kelin;
Colovati, Mileny E.;
Soares Pinho Cernach, Mirlene C.;
Bragagnolo, Silvia;
Melaragno, Maria Isabel

Publication type:

Case Study

Treatment of 153 Japanese patients with Q-switched alexandrite laser.

Published in:

2007

By:

Kagami, Shinji;
Asahina, Akihiko;
Watanabe, Rei;
Mimura, Yoshihiro;
Shirai, Akira;
Hattori, Naoko;
Watanabe, Takahiro;
Tamaki, Kunihiko

Publication type:

journal article

Predictive Genetic Testing in Children: Constitutional Mismatch Repair Deficiency Cancer Predisposing Syndrome.

Published in:

2014

By:

Bruwer, Zandrè;
Algar, Ursula;
Vorster, Alvera;
Fieggen, Karen;
Davidson, Alan;
Goldberg, Paul;
Wainwright, Helen;
Ramesar, Rajkumar

Publication type:

Report

The Etiology and Clinical Features of Non-CAH Gonadotropin-Independent Precocious Puberty: A Multicenter Study.

Published in:

2016

By:

Atay, Zeynep;
Yesilkaya, Ediz;
Erdeve, Senay Savas;
Turan, Serap;
Akin, Leyla;
Eren, Erdal;
Doger, Esra;
Aycan, Zehra;
Abali, Zehra Yavas;
Akinci, Aysşehan;
Siklar, Zeynep;
Ozen, Samim;
Kara, Cengiz;
Tayfun, Meltem;
Sari, Erkan;
Tutunculer, Filiz;
Karabulut, Gulcan Seymen;
Karaguzel, Gulay;
Cetinkaya, Semra;
Saglam, Halil

Publication type:

journal article

Extensive and Persistent Dermal Melanocytosis in a Male Carrier of Mucopolysaccharidosis Type IIIC (Sanfilippo Syndrome): A Case Report.

Published in:

Children, 2023, v. 10, n. 12, p. 1920, doi. 10.3390/children10121920

By:

Romagnuolo, Maurizio;
Moltrasio, Chiara;
Gasperini, Serena;
Marzano, Angelo Valerio;
Cambiaghi, Stefano

Publication type:

Article

COUNTING THE CALs.

Published in:

Community Practitioner, 2018, v. 91, n. 5, p. 25

By:

Sweeney, Leah

Publication type:

Article

Management of common neonatal problems.

Published in:

British Journal of Nursing, 2015, v. 24, n. 5, p. 258, doi. 10.12968/bjon.2015.24.5.258

By:

El-Radhi, A. Sahib

Publication type:

Article

Hyperpigmented spots at fundus examination: a new ocular sign in Neurofibromatosis Type I.

Published in:

2021

By:

Moramarco, Antonietta;
Mallone, Fabiana;
Sacchetti, Marta;
Lucchino, Luca;
Miraglia, Emanuele;
Roberti, Vincenzo;
Lambiase, Alessandro;
Giustini, Sandra

Publication type:

journal article

Retinal cafe-au-lait macules: A rare retinal finding in a patient with neurofibromatosis type 1.

Published in:

2019

By:

Venkatesh, Ramesh;
Jain, Kushagra;
Pereira, Arpitha;
Jain, Shreya;
Aseem, Aditya;
Mahendradas, Padmamalini;
Yadav, Naresh;
Jain, Shreya Dass;
Yadav, Naresh Kumar

Publication type:

journal article

Association of urticaria pigmentosa with café-au-lait spots, neurofibromas and neurofibroma-like neoplasms: a mere coincidence?

Published in:

2003

By:

Möhrenschlager, Matthias;
Engst, Reinhard;
Müller-Weihrich, Stefan;
Spiessl, Walter;
Rüdisser, Klaus;
Weigl, Lorenz B;
Jessberger, Berthold;
Braun-Falco, Markus;
Abeck, Dietrich;
Ring, Johannes

Publication type:

journal article

Response to Laser Treatment of Café au Lait Macules Based on Morphologic Features.

Published in:

2017

By:

Belkin, Daniel A.;
Neckman, Julia P.;
Jeon, Hana;
Friedman, Paul;
Geronemus, Roy G.

Publication type:

journal article

MCCUNE ALBRIGHT SYNDROME - ASSOCIATION OF FIBROUS DYSPLASIA, CAFÉ-AU-LAIT SKIN SPOTS AND HYPERTHYROIDISM - CASE REPORT.

Published in:

2016

By:

RAUS, IULIAN;
COROIU, ROXANA ELENA

Publication type:

Case Study

Is neurofibromatosis type 1 diagnosed in every patient who presents with café au lait macules? A single-center experience.

Published in:

Marmara Medical Journal, 2023, v. 36, n. 2, p. 192, doi. 10.5472/marumj.1302264

By:

EKER, Nursah;
TOKUC, Ayse Gulnur;
TUFAN, Burcu TAS;
SENAY, Emel

Publication type:

Article

Café au lait macules and vitiligo: A conflicting coexistence.

Published in:

Pigment International, 2023, v. 10, n. 3, p. 186, doi. 10.4103/pigmentinternational.pigmentinternational_28_22

By:

Palaniappan, Vijayasankar;
Sankarapandian, Jeyalakshmi;
Karthikeyan, Kaliaperumal

Publication type:

Article

SEGMENTAL NEUROFIBROMATOSIS 1: A 24-YEAR FOLLOW UP.

Published in:

2015

By:

Pisani, V.;
Bonifazi, E.

Publication type:

Case Study

Segmental neurofibromatosis type 1. Differences between the childhood and adult form.

Published in:

European Journal of Pediatric Dermatology, 2012, v. 22, n. 4, p. 257

By:

Pisani, V.;
Caniglia, A.;
Bonifazi, E.

Publication type:

Article

Giant café au lait macule in an infant.

Published in:

Indian Journal of Paediatric Dermatology, 2015, v. 16, n. 4, p. 268, doi. 10.4103/2319-7250.165672

By:

Tejaswi, Cherukuri;
Rangaraj, Murugaiyan;
Karthikeyan, Kaliaperumal

Publication type:

Article

Hypomelanosis of Ito associated with cafe-au-lait spot and angiomatous nevi.

Published in:

2015

By:

Geetha, K.;
Priya, G. Lakshmi;
Rameshwari, T.

Publication type:

Case Study

Pigmentation Disorders: Diagnosis and Management.

Published in:

2017

By:

PLENSDORF, SCOTT;
LIVIERATOS, MARIA;
DADA, NABIL

Publication type:

journal article

Type I Neurofibromatosis Complicated by Large Cell Neuroendocrine Carcinoma of the Lung.

Published in:

Turkish Thoracic Journal / Turk Toraks Dergisi, 2014, v. 15, n. 4, p. 168, doi. 10.5152/ttd.2014.4276

By:

Nadia, Amangar;
Rachida, Zahraoui;
Khaoula, Al Ataouna;
Mouna, Soualhi;
Ghali, Iraqi;
Eddine, Bourkadi Jamal

Publication type:

Article

Secondary Vascular Alterations in Diffuse and Plexiform Neurofibroma: An Impressive yet Little Known Morphologic Change.

Published in:

2014

By:

Pirola, Sara;
Oliff, Andrew

Publication type:

Case Study

Central precocious puberty in a girl with LEGIUS syndrome: an accidental association?

Published in:

Italian Journal of Pediatrics, 2021, v. 47, n. 1, p. 1, doi. 10.1186/s13052-021-01004-9

By:

Orlandi, Valentina;
Cavarzere, Paolo;
Palma, Laura;
Gaudino, Rossella;
Antoniazzi, Franco

Publication type:

Article

Picosecond 532-nm neodymium-doped yttrium aluminium garnet laser-a novel and promising modality for the treatment of café-au-lait macules.

Published in:

2018

By:

Artzi, Ofir;
Mehrabi, Joseph N.;
Koren, Amir;
Niv, Roni;
Lapidoth, Moshe;
Levi, Assi

Publication type:

journal article

Johanson–Blizzard's Syndrome with a Novel Mutation in UBR1 Gene.

Published in:

Journal of Neonatology, 2025, v. 39, n. 3, p. 287, doi. 10.1177/09732179241299957

By:

Banu S., Nasreen;
Vinnakota, Naga Chaitanya;
Alluwada, Lavanya;
Tripathi, Parijat Ram

Publication type:

Article

Newborn Wearing an Ascot Cap.

Published in:

Journal of Neonatology, 2023, v. 37, n. 3, p. 273, doi. 10.1177/09732179221142971

By:

Priyadarshi, Mayank;
Singh, Poonam;
Chaurasia, Suman;
Basu, Sriparna

Publication type:

Article

A 13-year-old girl with neurofibromatosis-1, scoliosis.

Published in:

2004

By:

Listernick, Robert

Publication type:

journal article

Wood's lamp fluorescence of dihydroxyacetone treated skin.

Published in:

Journal of the European Academy of Dermatology & Venereology, 2016, v. 30, n. 11, p. e125, doi. 10.1111/jdv.13401

By:

Jankowski, M.;
Nowowiejska, L.;
Czajkowski, R.

Publication type:

Article

Multiple hypo- and hyper-pigmentation: An example of twin spotting?

Published in:

2022

By:

Zhang, Li-wen;
Wu, Juan

Publication type:

Case Study